Overview
Microneedling: traditional, RF, and PRP
Microneedling uses fine needles to make tiny punctures in the skin, and the skin produces collagen as it heals (AAD). Three types are offered: traditional microneedling with a pen-style device such as SkinPen, radiofrequency (RF) microneedling, which also delivers heat through the needles (AAD), and PRP microneedling (sold as the “Vampire Facial”), which adds platelet-rich plasma made from your own blood. Each has a different evidence base and different safety questions.
This guide covers what the FDA has authorized, what the published evidence shows, and the Texas rules that apply.
| Attribute | What the sources say |
|---|---|
| Houston price | This site does not publish a Houston price range for microneedling. Ask the spa for the price of the specific treatment and whether it covers one session or a series. |
| Recovery | Redness, darker skin or a sunburn-like feeling usually fades in a few days to a week; wait 24 hours before makeup (AAD) |
| Sessions (acne scars) | 3 to 5 treatments, every 2 to 4 weeks (AAD) |
| Results | Full results usually take several months; a yearly maintenance session may be suggested (AAD) |
Mechanism
How microneedling works
The needles create controlled wounds in the dermis. A 2018 review in Dermatologic Surgery describes this controlled dermal wounding and stimulation of the wound-healing cascade as increasing collagen production, and reports improvement of scars, stretch marks and wrinkles with short recovery and limited side effects (Alster & Graham, Dermatol Surg 2018).
How the FDA regulates it. In 2018 the FDA classified the “microneedling device for aesthetic use” as a Class II device under 21 CFR 878.4430 (Federal Register, 83 FR 26575). That classification came from the FDA’s De Novo order for the SkinPen Precision System, a prescription device indicated to improve the appearance of facial acne scars in adults aged 22 or older (FDA DEN160029). The classification does not include devices intended to deliver cosmetics, drugs or biologics through the skin (FDA DEN160029). The FDA says it has authorized certain microneedling devices for facial acne scars, facial wrinkles and abdominal scars in patients 22 or older, and that products that do not penetrate the living layers of skin and only claim to exfoliate or improve appearance may not be devices (FDA). The FDA’s guidance on when a microneedling product is a device was finalized in November 2020 (FDA guidance).
Why that matters in Texas. Texas Medical Board rules treat nonsurgical medical cosmetic procedures, including the use of a prescription medical device for cosmetic purposes, as the practice of medicine (22 TAC §169.25). The rule does not name microneedling. TDLR lists microneedling (PRP injections/Vampire facials) as regulated by the Texas Medical Board (TDLR). See the Texas section below.
Traditional vs RF
Traditional microneedling vs. radiofrequency microneedling
Traditional microneedling relies on the needle punctures alone. RF microneedling also delivers heat through the needles, which the AAD says can increase collagen production; the AAD notes that some small studies suggest results similar to laser with less downtime, and that more research is needed (AAD). A 2025 systematic review of 16 studies (481 patients) concluded that fractional RF microneedling is likely effective for acne scars when used alone, and that more randomized trials are needed to set treatment parameters (Niaz et al., Clin Cosmet Investig Dermatol 2025).
The FDA calls RF microneedling a medical procedure, not a cosmetic treatment, and says the devices should not be used at home. In October 2025 it reported burns, scarring, fat loss, disfigurement and nerve damage with some uses (FDA).
Traditional microneedling devices
| Device | FDA authorization | Indication |
|---|---|---|
| SkinPen Precision System | De Novo DEN160029 (order dated March 1, 2018) | Facial acne scars, adults 22 or older (FDA) |
| SkinPen Precision System | 510(k) K202243 (April 2, 2021) | Neck wrinkles (Fitzpatrick II–IV) and facial acne scars (all skin types), adults 22 or older (FDA) |
Other pen devices are marketed under their own FDA records. Ask your provider which device they use and check its record in the FDA’s 510(k) and De Novo databases.
Radiofrequency microneedling devices
The RF devices below are cleared through the 510(k) process, most with a general indication for electrocoagulation and hemostasis in dermatologic procedures, not a specific cosmetic claim. The FDA advises asking your provider which device they plan to use (FDA).
| Device | FDA 510(k) | Cleared indication |
|---|---|---|
| Morpheus8 (InMode) | K192695 (Dec 27, 2019) | Electrocoagulation and hemostasis; at energy above 62 mJ/pin, limited to skin types I–IV (FDA) |
| Morpheus8 90 Applicator (InMode) | K240017 (June 13, 2024) | Coagulation/contraction of soft tissue or hemostasis; at energy above 62 mJ/pin, limited to skin types I–IV (FDA) |
| Vivace (Sung Hwan E&B) | K150409 (Jan 15, 2016) | See FDA record (FDA) |
| Secret RF (Ilooda) | K170325 (June 13, 2017) | Electro-coagulation and hemostasis (FDA) |
| Profound (Syneron Candela) | K161043 (Sept 12, 2016) | Electrocoagulation and hemostasis; dermal handpiece for facial wrinkles (FDA) |
| Genius (Lutronic) | K180945 (Dec 10, 2018) | Electrocoagulation and hemostasis (FDA) |
| Sylfirm X (VIOL) | K200185 (Apr 22, 2020); K213612 (June 23, 2022) | Electrocoagulation and hemostasis (FDA) |
Implants. Tell your provider about any implanted electronic device (such as a pacemaker) or metal implant before RF microneedling, and ask whether the device they use is suitable for you.
Skin Safety
Microneedling for darker skin tones
The AAD states that microneedling, including RF microneedling, is safe for all skin tones, and notes that research on RF microneedling in darker skin is limited (AAD). The FDA lists darker skin type among the reasons microneedling may not be suitable (FDA).
What the published evidence shows:
- A 2016 review in the Journal of the American Academy of Dermatology concluded that microneedling may have a more favorable safety profile in Fitzpatrick skin types IV–VI than conventional resurfacing such as dermabrasion, chemical peels and laser (Cohen & Elbuluk, JAAD 2016).
- A 2023 review of RF and RF microneedling in Fitzpatrick skin types III–VI found a low reported risk of scarring or hyperpigmentation, though many of the studies were of low quality (Syder et al., Dermatol Surg 2023).
- A 2026 meta-analysis of eight randomized trials (249 patients) found that fractional CO2 laser carried about 4.4 times the risk of post-inflammatory hyperpigmentation of RF microneedling for acne scars, though the laser improved scars more (Argobi et al., J Cosmet Dermatol 2026). That figure is for all patients in the trials, not only darker skin.
- In a study of 30 patients with skin types IV and V treated with a dermaroller for acne scars, five developed post-inflammatory hyperpigmentation and two developed tram-track scarring (Dogra et al., J Cosmet Dermatol 2014).
Questions to ask. Ask your provider how often they treat your skin type, how they adjust needle depth and settings for it, and to see photos of results on patients with similar skin.
PRP / Vampire Facial
PRP and the “Vampire Facial”
Platelet-rich plasma (PRP) is made from your own blood, which is drawn and spun in a centrifuge to concentrate the platelets. In PRP microneedling it is applied to the skin during treatment.
What the evidence shows. A 2019 systematic review of PRP for acne scars found that PRP combined with fractional ablative laser improves the appearance of acne scars, and described the evidence for PRP with microneedling as less supportive. The studies varied too much for the authors to run a statistical comparison (Hesseler & Shyam, JAAD 2019). The AAD says microneedling with PRP may be especially effective for acne scars (AAD).
FDA status. The FDA says microneedling devices are not approved for delivering blood products such as PRP, or for delivering cosmetics, topical medications, vitamin solutions or drugs (FDA).
The 2024 CDC report. In April 2024 the CDC published its investigation of PRP microneedling facials at an unlicensed spa in New Mexico. Five people were diagnosed with HIV between 2018 and 2023: four women who received services at the spa and the sexual partner of one of them. The CDC described it as the first investigation to associate HIV transmission with nonsterile cosmetic injection services (CDC MMWR). Inspectors found:
- Disposable electric desiccator tips cleaned by alcohol immersion and reused
- Unlabeled tubes of blood stored in the kitchen refrigerator, and unlabeled tubes of blood on a kitchen counter
- Unwrapped syringes in drawers, on counters and in regular trash cans
Of 198 former clients and sexual partners tested, no additional HIV infections and no hepatitis B or hepatitis C infections were found (CDC MMWR).
What to ask before a PRP microneedling appointment:
- Who draws your blood, and what license they hold.
- Whether a new needle cartridge is used for you. The FDA says re-use of a needle cartridge is unsafe, even if it is cleaned (FDA).
- How your blood is labeled, processed and stored.
- Whether a physician, PA or APRN is onsite or immediately available for emergency consultation, as Texas rules require for delegated procedures (22 TAC §169.26).
What to Expect
What to expect before, during, and after treatment
-
Before treatment
Tell your provider about all medications, including blood thinners and isotretinoin. The AAD says at least one month must pass after your last isotretinoin pill (AAD). Disclose any implanted device before RF microneedling. Protect your skin from the sun (AAD).
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Day of treatment
The device is passed over the skin. On some motorized devices the practitioner adjusts needle depth and speed (FDA). Ask whether a new needle cartridge is being used for you.
-
First days
Common effects listed by the FDA include redness, dryness, tightness, peeling, itching, bruising, bleeding and crusting (FDA). The AAD says redness, darker skin or a sunburn-like feeling usually fades in a few days to a week, and to wait 24 hours before applying makeup (AAD).
-
Weeks after
Protect your skin from the sun (AAD). Contact a licensed provider if you have problems or concerns after an RF microneedling procedure (FDA).
-
Months after
For acne scars, the AAD says 3 to 5 treatments every 2 to 4 weeks may be needed, full results usually take several months, and a dermatologist may suggest one maintenance session a year (AAD).
Houston Pricing
Houston pricing
This site does not publish a Houston price range for microneedling. Price depends on the type of microneedling and whether radiofrequency or PRP is added. Ask the spa for the price of the specific treatment and whether it covers one session or a series.
Combinations
How microneedling pairs with other treatments
Microneedling is sometimes scheduled alongside chemical peels, laser treatments, Botox or dermal fillers. This site does not publish spacing rules for combining them. Ask your provider whether the treatments can be done on the same day and how far apart to schedule them.
For acne scars, a 2026 meta-analysis found that fractional CO2 laser improved scars more than RF microneedling but caused more pain, longer redness and a higher risk of post-inflammatory hyperpigmentation (Argobi et al., J Cosmet Dermatol 2026).
Texas Law
How to choose a provider in Houston
Who regulates microneedling in Texas. TDLR lists microneedling (PRP injections/Vampire facials) as regulated by the Texas Medical Board (TDLR). Texas Medical Board rules treat nonsurgical medical cosmetic procedures, including the use of a prescription medical device for cosmetic purposes, as the practice of medicine (22 TAC §169.25). These rules took effect January 9, 2025 (Texas Medical Board).
When a physician delegates a procedure, the rules require:
- Before the procedure, a physician, or a PA or APRN acting under a physician’s delegation, establishes a practitioner-patient relationship with you (22 TAC §169.26).
- At least one person trained in basic life support is present while you are onsite, and a physician, PA or APRN is onsite or immediately available for emergency consultation (22 TAC §169.26).
- The delegation is made under a written order that names the delegating physician and covers patient selection, care, and complications and emergencies (22 TAC §169.27). The person performing the procedure must also sign and date a written protocol (22 TAC §169.26).
- The delegating physician’s name and Texas license number are posted in each public area and treatment room (22 TAC §169.28).
Estheticians. TDLR’s esthetician scope of practice does not list microneedling, and states that an esthetician cannot perform services other than those listed (TDLR). TDLR also says the facial treatments estheticians may perform do not include medical-type procedures that require the use of needles (TDLR).
Checking credentials:
- Delegating physician: find the posted name and license number, then check it on the Texas Medical Board’s Look Up a License page.
- Nurse: if a nurse is performing your treatment, check the license on the Texas Board of Nursing license verification page.
- Who is treating you: ask the identity and title of the person who will perform the procedure; the rules require this to be disclosed (22 TAC §169.26).
- For PRP: ask who draws your blood and how it is labeled and stored, and confirm a new needle cartridge is used (FDA).
Warning signs:
- No identifiable delegating physician, and no posted physician name and Texas license number (22 TAC §169.28)
- The operator cannot name the device being used (FDA)
- An esthetician offering microneedling (TDLR)
- Reused needle cartridges, or cartridges “cleaned” between clients (FDA)
- Unlabeled blood tubes or no clear answer about who draws and handles your blood (CDC MMWR)
- RF microneedling offered for home use (FDA)
Treatment Areas