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BOSS Instruments

BOSS INSTRUMENTS, LTD., INC. · Model 80-3658 · UDI-DI 00888515212596

HNF Prescription
10
510(k) clearances
385
Adverse events
2
Recalls
265
Facilities

Description

Stevens Tenot Sci, cvd, hvy, ribbon hndl

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2024-09-17MicroSurgical Technology IncDue to pin coming off of handles.

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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.