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

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PALAMED

FDA 510(k)
FDA Class 2 ·Orthopedic

Hi-Torque Proceed™

FDA UDI
ABBOTT VASCULAR INC.·08717648321382·Hi-Torque Proceed 220T Angled Guide Wire w/Hydr...

Graves Speculum X Large

FDA UDI
MEDGYN PRODUCTS, INC.·M803030904·Graves Speculum X Large 1 1/2" x 6 1/2" (38mm ...

LEONE SPA

FDA UDI
LEONE SPA·08033707065715·INTRAORAL ELASTICS 4,5 oz 5/16" blue

Ventilator

FDA UDI
Zoll Medical Corporation·00847946024130·CLAMP WITH DOVETAIL,CCLAW

LINEAR ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 10, 2019

PENADAPT 10

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

POLYMER COATED POWDER FREE LATEX EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

General Instruments

FDA UDI
ORTHOPEDIATRICS CORP.·00841132132463·SEAT POST CAP - LONG

General Instruments

FDA UDI
ORTHOPEDIATRICS CORP.·00841132150573·Seat, Split

Spica Table

FDA UDI
ORTHOPEDIATRICS CORP.·00841132135174·OP REPACKAGE BASE

RADIANALYZER¿ XPRESS¿

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC.·Product code DQK·November 17, 2017

8030904-1997-90002

FDA Adverse Event
Injury ·Product code DXC·September 16, 1997

8030904-1997-90001

FDA Adverse Event
Product code DXC·September 16, 1997

8030904-2005-00001

FDA Adverse Event
Injury ·RADI MEDICAL SYSTEMS AB·Product code DQX·August 26, 2005

DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVY·June 22, 2017

ASSURITY MRI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·December 7, 2022

HELICAL BLADE INSERTER

FDA Adverse Event
Malfunction ·SYNTHES BRANDYWINE·Product code LXH·April 2, 2013

SEBRA SEALER 2380 AND SEBRA SEALER HEAD 1105

FDA Adverse Event
Injury ·HAEMONETICS CORP.·Product code GKT·March 21, 2011

GE OEC 9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 17, 2008