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Hoyte Sacrocervicopexy Tip

Coopersurgical, Inc. · Model LH-SCERV-LRG · UDI-DI 00888937015263

HDL Prescription
2
510(k) clearances
19
Adverse events
1
Recalls
120
Facilities

Description

Hoyte Sacrocervicopexy Tip- Large

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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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.