29 results · 23ms · Sources: EU EUDAMED, US FDA

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HANSATOME MICROKERATOME

FDA 510(k)
FDA Class 1 ·Ophthalmic

Avitene

FDA UDI
Davol Inc.·00801741010491·EndoAvitene Microfibrillar Collagen Hemostat in...

Silverbolt/Mainframe

FDA UDI
Choice Spine, LP·10885862163486·

CORTICAL SCREW 3.5mm x 26.0mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665019698·

NIDO Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07315K0100600·Caddie, Modular Bone Screws

RITA STARBURST XLI ELECTROSURGICAL DEVICE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ALLROUND 55 LF

FDA 510(k)
FDA Class 2 ·Dental

M-SERIES DC POWER SUPPLY

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·May 25, 2012

REMSTAR AUTO M SERIES

FDA Adverse Event
Injury ·RESPIRONICS, INC.·Product code BZD·April 14, 2024

OPTETRAK LOGIC KNEE COMPONENTS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·February 18, 2025

AXSYM DIGOXIN III

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·March 12, 2013

3M IOBAN ANTIMICROBIAL INCISE DRAPE

FDA Adverse Event
3M COMPANY·Product code KKX·February 25, 2011

LOGIC TIBIA PS MOD INSRT SZ 6 11MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 24, 2024

LOGIC KNEE COMPONENTS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 7, 2026

LOGIC TIBIA PS MOD INSRT SZ 6 9MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 17, 2023

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 1, 2024

LOGIC TIBIA PS MOD INSRT SZ 6 9MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·January 17, 2024

MENTOR SMOOTH ROUND HIGH PROFILE

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code FWM·June 22, 2018

LOGIC TIBIA PS MOD INSRT SZ 6 11MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·September 8, 2023