EJG
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Forceps, Rubber Dam Clamp
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 872.6300
- Medical specialty
- Dental
- Flags
- GMP exempt
- Adverse events (MAUDE)
- 2003: 2 · 2004: 2
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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| Record | Firm | Date | Builder |
|---|---|---|---|
| CLAMP FORCEPS (K780743) | Hygienic Dental Mfg., Co., The | 1978-05-12 | + Add |
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