SkinStylus SteriLock MicroSystem (MP1209SL)
K-Number: K253002 · 2026-02-19
ApplicantEsthetic Medical, Inc.
Decision Date2026-02-19
Product CodeQAI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
SkinStylus SteriLock MicroSystem (MP1209SL) is a medical device manufactured by Esthetic Medical, Inc.. It received FDA 510(k) clearance on 2026-02-19 under approval number K253002. The device is classified under product code QAI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Esthetic Medical, Inc.. The 510(k) number is K253002.
When was SkinStylus SteriLock MicroSystem (MP1209SL) approved by the FDA?
SkinStylus SteriLock MicroSystem (MP1209SL) received FDA 510(k) clearance on 2026-02-19, under approval number K253002.
What company makes SkinStylus SteriLock MicroSystem (MP1209SL)?
SkinStylus SteriLock MicroSystem (MP1209SL) is manufactured by Esthetic Medical, Inc..
What is the FDA product code for SkinStylus SteriLock MicroSystem (MP1209SL)?
The FDA product code for SkinStylus SteriLock MicroSystem (MP1209SL) is QAI.
Other Devices by Esthetic Medical, Inc.
Related Devices (Code: QAI)
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.