14 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.

TUM-E-VAC

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

P.F.C. SIGMA

FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295244912·P.F.C. SIGMA STABILIZED PLUS TIBIAL INSERT TRIA...

GuideMia Ortho+

FDA 510(k)
FDA Class 2 ·Dental

AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERS

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

GEENEN PANCREATIC STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·July 9, 2014

EEA 28MM SINGLE-USE STAPLER

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·June 1, 2015

EEA31

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·August 31, 2015

PREMIUM PLUS CEEA* 28 INSTR. W/TILT-TOP*

FDA Adverse Event
Injury ·COVIDIEN MEDICAL PRODUCTS (SHANGHAI) MAN·Product code GDW·November 4, 2015

VERTEBRAL BODY SPREADER- ANGLED

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HTD·February 14, 2013

VISIAN ICL (IMPLANTABLE COLLAMER LENS)

FDA Adverse Event
Injury ·STAAR SURGICAL CO.·Product code MTA·January 12, 2011

GREENLIGHT MOXY FIBER OPTIC

FDA Adverse Event
Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·July 29, 2014

DST SERIES ORVIL AUTOMATIC 25MM DEVICE

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·April 25, 2016

EEA 31MM SINGLE-USE STAPLER

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GAG·December 11, 2015

BIOMET StageOne, Shoulder Cement Spacer Mold 14 MM, 58 X 24 X 64 MM, Silicone, Sterile, Item 431414.

FDA Enforcement
Class II ·Terminated·Biomet, Inc.·April 15, 2020