FDA Device Intelligence
HomeSONTEC INSTRUMENTS, INC. › PIN DRIVER/BONE TAMP

PIN DRIVER/BONE TAMP

SONTEC INSTRUMENTS, INC. · Model 1103-2011 · UDI-DI 00192896052154

GFC Prescription
2
510(k) clearances
101
Adverse events
2
Recalls
87
Facilities

Description

PIN DRIVER/BONE TAMP SINGLE ENDED FLAT TIP

Recalls

DateFirmReason
2014-09-09Zimmer, Inc.The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use of the screw in cortical bone, and corresponding stripping of the 2.5mm Persona Hex Driver.
2013-05-30Exactech, Inc.When torque is applied to the Articulated Driver at the maximum angle, the cross pin may shift out of position, potentially leading to disassembly of the instrument.

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.