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DENTECH

DENTECH CORPORATION · Model 50580003 · UDI-DI 04560218660510

EEF
3
510(k) clearances
301
Adverse events
1
Recalls
98
Facilities

Recalls

DateFirmReason
2021-04-21Dentech Corp.Removing parts for safety reasons due to possible breakage.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.