58 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

INSTRU-SAFE INSTRUMENT PROTECTION SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

BIOMET KNEE SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304002920·

Biomet® Knee System

FDA UDI
Biomet Orthopedics, LLC·00887868558894·

Biomet® Knee System

FDA UDI
Biomet Orthopedics, LLC·00887868248054·

3M™ Unitek™

FDA UDI
3M UNITEK CORPORATION·00652221037589·Unitek(TM) Bicuspid Band General Purpose Narrow...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613068462·Buck Ear Curette, Angled, Sharp, Size 0, 1.5mm ...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613068479·Buck Ear Curette, Angled, Sharp, Size 00, 1mm O...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613068486·Buck Ear Curette, Angled, Sharp, Size 1, 2mm Ou...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613068493·Buck Ear Curette, Angled, Sharp, Size 2, 2.5mm ...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613068509·Buck Ear Curette, Angled, Sharp, Size 3, 3mm Ou...

Verteloc Spinal System

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215129040·

CX50 DIAGNOSTIC ULTRASOUND SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

MULTIX FUSION

FDA 510(k)
FDA Class 2 ·Radiology

MAXIM CONSTRAINED TIBIAL BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 16, 2018

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·June 5, 2025

MAXIM CONSTRAINED TIBIAL PLATE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 16, 2018

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

STAB HIP PC 12-22 LG W/CS

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LZO·June 22, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

VNGD TI FEM CR 60MM LT

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·December 20, 2016