15 results · 22ms · 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.

OPTIMUS FUSION: SLT, YAG AND YAG/SLT

FDA 510(k)
FDA Class 2 ·Ophthalmic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·00636257125281·20-30 MV FOR MEN CLSC CALF STD NAVY VI

Gyrus ACMI

FDA UDI
Gyrus ACMI, LLC·00821925015265·MCGEE PISTON 3.75 MM LENGTH .5 MM DIAMETER PLAT...

CAPTURED SCREW ASSEMBLY

FDA UDI
Biomet Orthopedics, LLC·00887868004070·

Hayden Medical

FDA UDI
Hayden Medical, Inc.·00840319704806·Bengolea Forceps 10-1/4" (25.6cm), curved

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197053679·Baby-Crile artery forceps, 1x2 14.0cm...

SYNTHES (USA) LATERAL ENTRY FEMORAL NAIL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

MULTICODE - RTX HERPES SIMPLEX VIRUS 1 AND 2 KIT, MODEL 3711

FDA 510(k)
FDA Class 2 ·Microbiology

WAVEWRITER ALPHA 16

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 29, 2024

GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 6/12 MM L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 10, 2021

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·October 3, 2014

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NKB·May 31, 2013

LIFEVEST WCD 4000 SYSTEM

FDA Adverse Event
Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 15, 2011

6.5MM TI RECON SCREW WITH T25 STARDRIVE 95MM

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·April 23, 2018

6.5MM TI RECON SCREW WITH T25 STARDRIVE 105MM

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·April 23, 2018