Performance Health 7507
Performance Health 7507 is a Class I device made by Asp Global, LLC, listed in FDA GUDID since 15 Aug 2022 (UDI-DI 00840216105645), registry data as of 23 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 | Number00840216105645 | Date15 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 00840216105645
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Performance Health
- Generic name
- Manual goniometer
- Model / reference
- 7507
- Primary DI / UDI-DI
- 00840216105645
- FDA product code
- KQW
- GMDN term
- Manual goniometer
- Device class
- Class I
- Regulation number
- 888.1520
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code KQW (Goniometer, Nonpowered).
- GONIOMETER, INTER. STAND. LARGE, BK7514 by Fred Sammons, Inc.
- HAND HELD GONIOMETER by Chattanooga Group, Inc.
- FINGER BONIOMETER BK7506 by Fred Sammons, Inc.
- Humelock Reversed Shoulder 902-0002 by FX SOLUTIONS
- THE TELOS EQUIPMENT by The Telos Co.
- THE (CROM) TESTER by Twin City Surgical, Inc.
- DOBBHOFF(R) RETRIEVAL FORCEPS by BIOSEARCH MEDICAL PRODUCTS, INC.
- O'BRIEN GONIOMETER by Sgarlato Laboratories, Inc.