EJX
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Anchor, Preformed
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 872.3130
- Medical specialty
- Dental
- Adverse events (MAUDE)
- 1992: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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| Record | Firm | Date | Builder |
|---|---|---|---|
| ZX-27 (K133088) | M&M Dental Studio, Inc. | 2015-01-02 | + Add |
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Every clearance here is in the API, with alerts when new ones post.