15 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Zyston Strut Open Titanium Spacer System
FDA 510(k)
FDA Class 2
·Orthopedic
ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020
ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020
NA
FDA UDI
KEY SURGICAL, INC.·10849771049705·Steinmann Pins, Single trocar, 3 shank end, .15...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293531·
Steinmann pin w. trocar/3-shank 4.0mm/229mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM714950·Steinmann pin w. trocar/3-shank
4.0mm/...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484924·Steinmann pin w. trocar/3-shank _x000D_...
SACRO-ILIAC SCREW SYSTEM SI-JOINT SCREW 10X55
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code OUR·October 8, 2019
EXPEDIUM 4.5MM SPINE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
COOK GI ENDOSCOPIC INJECTION GEL KIT, GEL-S, GEL-N, GEL-H, GEL-K
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CONTAK RENEWAL
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 21, 2011
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013
CELL-DYN WBC REAGENT A
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·September 17, 2008
SACRO-ILIAC SCREW SYSTEM SI-JOINT SCREW 10X40
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code OUR·February 5, 2021
CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c. 21-2120-0105-06L d. 21-2120-0105-07L e. 21-2120-0105-08L f. 21-2120-0105-12L g. 21-2120-0105-13L h. 21-2120-0105-14L i. 21-2120-0105-15L j. 21-2120-0105-17L k. 21-2120-0105-50L l. 21-2127-0105-02L m. 21-2127-0105-06L n. 21-2127-0105-50L
FDA Enforcement
Class I
·Terminated·Smiths Medical ASD Inc.·October 27, 2021