Stryker LLS-050
Stryker LLS-050 (INV-LLS-2000HPAK) is a Class II device made by Sunoptic Technologies, listed in FDA GUDID since 15 May 2025 (UDI-DI 00855373008029), 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 | Number00855373008029 | Date15 May 2025 | StatusListed |
Official records
- AccessGUDID record 00855373008029
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Stryker
- Generic name
- General-purpose light source
- Model / Ref / Catalog
- LLS-050, INV-LLS-2000HPAK
- Primary DI / UDI-DI
- 00855373008029
- FDA product code
- FCW
- GMDN term
- General-purpose light source
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code FCW (Light Source, Fiberoptic, Routine).
- STRYKER LED LIGHTSOURCE by Stryker Corp.
- COLDLIGHTSOURCE PL3000 by Fiber Imaging Technologies, Inc.
- POWER LED 175 by Karl Storz Endoscopy-America, Inc.
- 10970AE by Karl Storz SE & CO. KG
- Olympus WA97020A by Olympus Winter & Ibe GmbH
- PRESCOTT'S LIGHT SOURCE MODEL NO. II-150 by Iba/Griffith
- TL005 by Karl Storz SE & CO. KG
- NOVAPROBE LED LIGHT SOURCE by Novaprobe Incorporated
- R.L. MEDICAL TWIN LIGHT SOURCE by Tridak Division of Indicon, Inc.
- PEDIATRIC ILLUMINATING URETERAL by Van-Tec, Inc.