34 results
·
19ms
·
Sources: EU EUDAMED, US FDA
EZ VEIN INFLATABLE TOURNIQUET
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
N/A
FDA UDI
HANS RUDOLPH, INC.·00874750006861·HTR SHELL/CABLE/CONN ASSY 8420
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024493704·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00846795001293·
ADVIA CHEMISTRY REAGENTS, AND ADVIA CHEMISTRY B2-MICROGLOBULIN CALIBRATOR
FDA 510(k)
FDA Class 2
·Immunology
NEW STETIC ACRYLICS
FDA 510(k)
FDA Class 2
·Dental
MUST PEDICLE SCREW SYSTEM - SCREW DRIVER
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL, SA·Product code LZO·July 24, 2014
G7 SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PBI·June 2, 2017
AVAN CMNTD SHELL SS 50MM
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LZO·April 24, 2026
MODULAR CUP SYSTEM, RIMCUP
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
AVAN CMNTD SHELL SS 50MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·January 21, 2026
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 14, 2013
DUROM ACETABULAR COMPONENT
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·September 17, 2014
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·June 3, 2011
RINGLOC MODULAR ACETABULAR SYSTEM (SPIDERCUP, RIMCUP, BATCUP)
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·October 2, 2018
G7 BONEMASTER LTD ACET SHL 58G
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JDI·September 23, 2019
G7 FINNED BM 3 HOLE SHELL 48C
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JDI·May 16, 2018