LightScalpel LSH-LSLB
LightScalpel LSH-LSLB (LS9029-02) is a Class II device made by Lightscalpel Inc, listed in FDA GUDID since 21 Oct 2022 (UDI-DI 00851842007654), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00851842007654 | Date21 Oct 2022 | StatusListed |
Official records
- AccessGUDID record 00851842007654
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- LightScalpel
- Generic name
- Laser adaptor
- Model / Ref / Catalog
- LSH-LSLB, LS9029-02
- Primary DI / UDI-DI
- 00851842007654
- FDA product code
- GEX
- GMDN term
- Laser adaptor
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code GEX (Powered Laser Surgical Instrument).
- BWF-5 Medical Laser Series by LITECURE LLC
- CLEAR+BRILLIANT TOUCH® Laser System by Solta Medical, Inc.
- Laser Gas Mixture by Tri-Gas, Inc.
- IPG Medical Thulium Fiber Lasers, Surgical Fibers, and Accessories by IPG Medical Corporation
- Palomar Aspire Laser Platform by Palomar Medical Products, Inc.
- SPECTRA VRMIII Q-SWITCHED ND: YAG LASER SYSTEM AND DYE HANDPIECES by Lutronic Corporation
- AURORA SR by SYNERON MEDICAL LTD
- DuraLazeTM HoLEP Laser Fiber by Medkey, LLC
- LATERALASE by TRIMEDYNE, INC.
- Lumenx Model GAT-577 Pulsed Dye Laser by Phase-R Corp.