18 results · 30ms · 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.

FFX Facet Fixation System

FDA 510(k)
FDA Unclassified ·Unknown

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112885·CORNEAL TREPHINE BLADE6.75MM

COLLECT.NO.QAS KNEE IMPLANTS COLUMBUS

FDA Adverse Event
Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code KRO·November 21, 2017

NA

FDA UDI
aap Implantate AG·04042409193187·Juxta-articular Radiusplate WSP 2.5, 5/3-Hole, ...

MicroSpot Handpiece

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

OMRON AUTOMATIC BLOOD PRESSURE MONITOR, MODEL HEM-741CREL

FDA 510(k)
FDA Class 2 ·Cardiovascular

AE-QAS-K521-53

FDA Adverse Event
Injury ·AESCULAP AG·Product code JWH·December 19, 2024

AS COLUMBUS REV F TIB.OFFSET CEMENT.T2+

FDA Adverse Event
Injury ·AESCULAP AG·Product code JWH·March 20, 2023

AS COLUMBUS REV F FEMUR CEMENTED F4L

FDA Adverse Event
Injury ·AESCULAP AG·Product code JWH·March 20, 2023

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 16, 2011

530G INSULIN PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·November 14, 2014

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 25, 2013

COLLECT.NO.QAS KNEE IMPLANTS COLUMBUS

FDA Adverse Event
Injury ·AESCULAP AG·Product code JWH·June 22, 2021

COLLECT.NO.QAS KNEE IMPLANTS COLUMBUS

FDA Adverse Event
Injury ·AESCULAP AG·Product code JWH·June 22, 2021

COLUMBUS

FDA Adverse Event
Injury ·AESCULAP AG·Product code OOG·December 1, 2023

COLLECT.NO.QAS KNEE IMPL.MISC./UNKNOWN

FDA Adverse Event
Injury ·AESCULAP AG·Product code JWH·March 5, 2021

COLUMBUS

FDA Adverse Event
Injury ·AESCULAP AG·Product code OOG·December 1, 2023

Exactech Equinoxe GLENOID,KEELED, CEMENTED, mates with 47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-01-12, b) Medium, Item Number 314-01-13, c) Large, Item Number 314-01-14, Shoulder Arthroplasty

FDA Enforcement
Class II ·Ongoing·Exactech, Inc.·April 10, 2024