18 results
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30ms
·
Sources: EU EUDAMED, US FDA
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