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NORDENT MANUFACTURING INC

NORDENT MANUFACTURING INC · Model M4SDOZ · UDI-DI 00840018604797

EAX
10
510(k) clearances
47
Adverse events
1
Recalls
375
Facilities

Description

MIRRORS,SS,FS,#4,BOX OF DOZEN

Recalls

DateFirmReason
2021-03-23Sunstar Americas, Inc.Product may be contaminated with Burkholderia contaminans.

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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.