FDA Device Intelligence
Home › SONTEC INSTRUMENTS, INC. › SOFT WIRE/CABLE CUTTER

SOFT WIRE/CABLE CUTTER

SONTEC INSTRUMENTS, INC. · Model 1103-128B · UDI-DI 00192896096875

HXZ Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
247
Facilities

Description

SOFT WIRE/CABLE CUTTER TUNGSTEN CARBIDE BLADES

Recalls

DateFirmReason
2020-11-20Zimmer Biomet, Inc.Device has the potential for fracture during use.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.