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American Eagle Instruments

AMERICAN EAGLE INSTRUMENTS, INC. · Model AEAF34-35 · UDI-DI 00841013100017

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

Description

ANGLE FORMER 34-35 (7-80-2.5-9)

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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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.