FDA Device Intelligence
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Integra® Miltex®

INTEGRA LIFESCIENCES PRODUCTION CORPORATION · Model PM-740 · UDI-DI 10381780464419

FSE Prescription
10
510(k) clearances
28
Adverse events
1
Recalls
50
Facilities

Description

Integra® Miltex® Surgical Hand Table, Aluminum 8" x 6-1/4"

Recalls

DateFirmReason
2006-05-15Stryker Medical Div. of Stryker CorporationAn incorrect pin may have been used during assembly and therefore the device may give way during use.

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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.