18 results · 29ms · Sources: EU EUDAMED, US FDA

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SeaSpine Cambria System

FDA 510(k)
FDA Class 2 ·Orthopedic

K-Wire and Steinmann Pin Dispensers

FDA UDI
KEY SURGICAL, INC.·00849771046370·K-Wire and Steinmann Pin Dispensers, Dispensing...

OSE

FDA UDI
ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042121010·Round Buccal Tubing - .045

STOCKERT S5 SYSTEM AND GAS BLENDER AND SORIN C5 SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

SYNTHES CHRONOS COMPOSITE

FDA 510(k)
FDA Class 2 ·Orthopedic

TRULIANT PS CEM FEM PS CEM RIGHT SZ 4.5

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·August 15, 2024

BD INTIMA-II Y 20GAX1.16IN PRN/EC SLM

FDA Adverse Event
Malfunction ·BD SUZHOU (MDS)·Product code FOZ·February 25, 2025

ELECTRONIC GAS BLENDER

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025

STOCKERT S3 GAS BLENDER

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014

8.0MM DRILL BIT FOR DHS/DCS TRIPLE REAMER

FDA Adverse Event
Malfunction ·SYNTHES HAGENDORF·Product code HTW·October 14, 2014

PROSTAR XL SUTURE-MEDIATED CLOSURE

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·June 14, 2013

5.0MM LOCKING SCREW

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·July 8, 2011

S3 GAS BLENDER SYSTEM

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017

S3 GAS BLENDER SYSTEM

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017

S3 ELECTRONIC GAS BLENDER

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·December 19, 2024

SORIN S3 GAS BLENDER

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTX·February 25, 2015

BD INTIMA-II Y 20GAX1.16IN PRN/EC SLM

FDA Adverse Event
Malfunction ·BD SUZHOU (MDS)·Product code FOZ·March 19, 2025

TRU CC FEMORAL SIZE 1 LEFT

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 15, 2025