KXR
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Applicator, Resin
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 872.3140
- Medical specialty
- Dental
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| DENTAL SYRINGE SYSTEM-VARIOUS STYLES (K832662) | Centrix, Inc. | 1983-10-04 |
| BRUSH, APPLICATOR (K781098) | 3M Company | 1978-09-29 |
| CERAMIST BRUSH (K770160) | Deringer-Ney, Inc. | 1977-01-31 |
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Every clearance here is in the API, with alerts when new ones post.