gSource gS 74.2109
gSource gS 74.2109 is a Class I device made by Gsource, LLC., listed in FDA GUDID since 2 Nov 2020 (UDI-DI 00840314238313), 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 | Number00840314238313 | Date2 Nov 2020 | StatusListed |
Official records
- AccessGUDID record 00840314238313
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- gSource
- Generic name
- Manual goniometer
- Model / Ref / Catalog
- gS 74.2109
- Primary DI / UDI-DI
- 00840314238313
- FDA product code
- KQW
- GMDN term
- Manual goniometer
- Device class
- Class I
- Regulation number
- 888.1520
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code KQW (Goniometer, Nonpowered).
- THE TELOS EQUIPMENT by The Telos Co.
- THE (CROM) TESTER by Twin City Surgical, Inc.
- GONIOMETER, MED. INTER. STAND. BK-7512 by Fred Sammons, Inc.
- DOBBHOFF(R) RETRIEVAL FORCEPS by BIOSEARCH MEDICAL PRODUCTS, INC.
- BK-7511 BRASS GONIOMETER by Fred Sammons, Inc.
- O'BRIEN GONIOMETER by Sgarlato Laboratories, Inc.
- HAND HELD GONIOMETER by Chattanooga Group, Inc.
- Humelock Reversed Shoulder 902-0002 by FX SOLUTIONS