NGR
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Tester, Stiffness, Cartilage, Arthroscopic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.1100
- Medical specialty
- Orthopedic
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ACTAEON PROBE (K013429) | Osteobiologics, Inc. | 2002-01-11 |
| ARTSCAN CARTILAGE STIFFNESS TESTING DEVICE (K010303) | Artscan Medical Innovations | 2001-09-11 |
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Every clearance here is in the API, with alerts when new ones post.