LGG
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Instrument, Cast Application/Removal, Manual
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.5980
- Medical specialty
- Orthopedic
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| PLASTER STAND (K870100) | Orthopedic Systems, Inc. | 1987-01-28 |
| 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF (K851786) | Artiberia | 1985-07-09 |
| MODULAR EXTREMITY CASTING SUPPORT (K834384) | Buckman Co., Inc. | 1984-01-30 |
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Every clearance here is in the API, with alerts when new ones post.