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HU-FRIEDY MFG. CO., LLC · Model RDCM2X · UDI-DI 10889950104993
3
510(k) clearances
301
Adverse events
1
Recalls
98
Facilities
Description
Rubber Dam Clamp #2, Black Line
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-04-21 | Dentech Corp. | Removing parts for safety reasons due to possible breakage. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.