KTD
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Orthosis, Abdominal
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 890.3490
- Medical specialty
- Physical Medicine
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ABDOMINAL BINDER (K823663) | Warm & Form, Orthopedic Materials | 1982-12-30 |
| ABDOMINAL BINDER (K823164) | Warm & Form, Orthopedic Materials | 1982-11-16 |
| ABDOMINAL BELT (K780229) | Biomet, Inc. | 1978-03-02 |
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Every clearance here is in the API, with alerts when new ones post.