24 results
·
25ms
·
Sources: EU EUDAMED, US FDA
MID-500
FDA 510(k)
FDA Class 2
·General Hospital
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117346·Modular Knee Stem Pilot 11mm x 75mm
Arthrex®
FDA UDI
ARTHREX, INC.·00888867060333·ECLIPSE HUMERAL HEAD EXTRACTOR
AHBPPRESS ABSORBABLE HEMOSTATIC BONE PUTTY
FDA 510(k)
FDA Unclassified
·Unknown
UNIPORT SELF-CONTAINED PORTABLE DENTAL UNIT
FDA 510(k)
FDA Class 1
·Dental
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·December 16, 2024
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·October 31, 2022
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·September 8, 2025
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·November 20, 2024
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·May 25, 2024
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·May 15, 2024
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·November 7, 2024
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·June 5, 2024
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·March 12, 2021
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·March 12, 2021
ECLIPSE HUMERAL HEAD EXTRACTOR
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code MDM·June 20, 2022
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Malfunction
·WAVELIGHT GMBH·Product code LZS·December 22, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 17, 2014
UNK
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MDM·September 26, 2025