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HU-FRIEDY MFG. CO., LLC · Model CV5651 · UDI-DI 10889950045708

EKH
3
510(k) clearances
17
Adverse events (1 deaths)
1
Recalls
96
Facilities

Description

D5/D6 Discoid

Recalls

DateFirmReason
2017-04-20Almore International IncMicrofil Composite Instruments were distributed with a sterile symbol on their packaging label inserts, indicating that the products are sold as sterile devices. These products are

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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.