SkinStylus SteriLock MicroSystem (MP1209SL)
K-Number: K253002 · 2026-02-19
Device Summary
Frequently Asked Questions
What is the SkinStylus SteriLock MicroSystem (MP1209SL)?
SkinStylus SteriLock MicroSystem (MP1209SL) is a medical device that received FDA 510(k) clearance on 2026-02-19. The listed applicant is Esthetic Medical, Inc.. The 510(k) number is K253002.
When did SkinStylus SteriLock MicroSystem (MP1209SL) receive FDA 510(k) clearance?
SkinStylus SteriLock MicroSystem (MP1209SL) received FDA 510(k) clearance on 2026-02-19, under 510(k) number K253002.
Who is the listed applicant for SkinStylus SteriLock MicroSystem (MP1209SL)?
The FDA 510(k) record lists Esthetic Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SkinStylus SteriLock MicroSystem (MP1209SL)?
The FDA product code for SkinStylus SteriLock MicroSystem (MP1209SL) is QAI.
Other records listing Esthetic Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QAI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.