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

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INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Bio2 Technologies

FDA UDI
BIO2 TECHNOLOGIES, INC.·B01010000391·VITRIUM E 18 x 9

CoRoent

FDA UDI
Nuvasive, Inc.·00887517406194·CoRoent LI Inserter, Short

Tempo

FDA UDI
i-SENS, Inc.·00810011730069·Tempo lancet (50T/pack)

AeroPace Handheld Controller

FDA UDI
Lungpacer Medical USA Inc.·00810073210042·

QB1 NMES System

FDA UDI
Motive Health, Inc.·00854816006141·QB1 NMES System; SMALL, SHORT, LEFT

Panama™

FDA UDI
FLOSPINE LLC·B1830830000390·3-Level, 39mm Cervical Plate

Canaveral®

FDA UDI
FLOSPINE LLC·B183170000390·Screw Tap, 9.5mm

SINGLE SIZE TENDON SPACER

FDA 510(k)
FDA Class 2 ·Orthopedic

SPIRAL RADIUS RODDING SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

6000039-2001-00055

FDA Adverse Event
Injury ·Product code LIT·December 13, 2001

NAVIGUIDE GUIDE WIRE

FDA Adverse Event
Injury ·MEDI-TECH·Product code DQX·July 23, 1998

NAVIGUIDE GUIDE WIRE

FDA Adverse Event
Injury ·MEDI-TECH·Product code DQX·July 23, 1998

Transcatheter Septal Occluder

FDA Pre-Market Approval
FDA Class 3 ·THE AMPLATZER(R) SEPTAL OCCLUDER (ASO) AND THE AMPLATZER EXCHANGE SYSTEM

OCCLUSION BALLOON CATHETER

FDA Adverse Event
Injury ·MEDI-TECH·Product code LIT·July 20, 2000

OCCLUSION BALLOON CATHETER

FDA Adverse Event
Malfunction ·MEDI-TECH·Product code LIT·July 20, 2000

ARCHITECT IPTH

FDA Adverse Event
Malfunction ·ABBOTT GERMANY·Product code CEW·March 12, 2013

SOFT-VU ANGIOGRAPHIC CATHETER

FDA Adverse Event
Malfunction ·ANGIODYNAMICS·Product code DQO·February 18, 2011

INDURA

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code LKK·February 15, 2008

NUVASIVE COROENT PROCEDURE

FDA Adverse Event
Malfunction ·NUVASIVE, INC.·Product code MQP·April 11, 2013