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A-dec

A-DEC, INC. · Model 12.0910.13 · UDI-DI 10194665001735

DYN
10
510(k) clearances
100
Adverse events (1 deaths)
0
Recalls
151
Facilities

Description

SE,Autoclavable,CE,Gray 3,12 FT

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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.