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SAIPH®

MATORTHO LTD · Model 293-704 · UDI-DI 05055455519411

FWH Prescription
1
510(k) clearances
12
Adverse events
1
Recalls
2
Facilities

Description

Saiph® Trial Bearing Yellow. Left.18mm

Recalls

DateFirmReason
2012-07-10Berchtold Corp.Defective camera: There is a possibility that the connection of the wires to the connector may become loose, causing image distortion or loss.

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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.