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AESCULAP

AESCULAP, INC. · Model FF086R · UDI-DI 04046955074716

HAE Prescription
10
510(k) clearances
482
Adverse events (1 deaths)
2
Recalls
64
Facilities

Description

KERRISON Bone Punch conventional, 90 °, upwards cutting, 8", (205 mm), width: 3 mm, opening width: 15 mm, without ejector, standardnon-sterile, reusable

Recalls

DateFirmReason
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.

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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.