65 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Shiley Adult Flexible Tracheostomy Tube Cuffless, Reusable Inner Cannula, Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, Reusable Inner Cannula
FDA 510(k)
FDA Class 2
·Anesthesiology
AGXO
FDA UDI
Oticon A/S·05707131280947·H160V2, BTE 13 WL 100 SGR AGXO
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868344381·
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304008502·
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100127·KRATZ-BARRAQUER SPECULUM RIGHT EYE
750C SERIES MONITOR, MODELS 750C-2MS, 750CM-2MS, 750C-NNL, 750CM-2NL, 750C-3MS, 750CM-3MS, 750C-3NL, 750CM-3NL
FDA 510(k)
FDA Class 2
·Cardiovascular
SYMBIA.NET
FDA 510(k)
FDA Class 2
·Radiology
BIOMET ARCOM AP PATELLA 3-PEG
FDA Adverse Event
Malfunction
·BIOMET, INC.·Product code JWH·May 20, 2008
BIOMET CC I-BEAM TRAY 83MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
VNGD CR TIB BRG 14X79/83
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
BIOMET ARCOM 3 PEG/POST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
VANGUARD CR ILOK FEM-LT 75
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
INGENIO
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 8, 2014
TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·June 6, 2013
ASR ACETABULAR IMPLANT 58
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 29, 2011
VANGUARD KNEE SYSTEM CR TIBIAL BEARING DCM ARCOM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·October 14, 2016
BMET ARCOM AP PAT 3PST 37MM LG
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·September 27, 2018
MAXIM ILOK ANA PRI FML 70 RT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·March 1, 2017
BIOMET CC I-BEAM TRAY 83MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·September 27, 2018
BIOMET INTERLOK FIXED CRUCIATE TIBIAL PLATE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 19, 2018