17 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PowerMidline Catheter
FDA 510(k)
FDA Class 2
·General Hospital
Clinician's Choice® Low Viscosity Tubes & Plugs
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002257·Dental material injection cannula, single-use
Mouthpiece, Disposable, 1 1/16" OD, 3.25" L
FDA UDI
A-M SYSTEMS, LLC·00817081023879·Mouthpiece, Disposable, 1 1/16" OD, 3.25" L
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702616279·ELVAREX 2/KNEE HIGH/SLANT-OPEN TOE-ELEPHANTIASI...
II Ring Retractor
FDA UDI
Automated Medical Products Corp.·00810118342585·Richardson Retractor 1" x 1 1/2"
PAJUNKS STIMULONG TSUI-METHOD SET
FDA 510(k)
FDA Class 2
·Anesthesiology
HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 25, 2025
PAINSMART IOD
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·May 13, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014
VANGUARD XP-XP MEDIAL BEARING TIBIAL TRAY E1 ANTIOXIDANT INFUSED
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBH·July 2, 2018
VANGUARD XP-XP LATERAL BEARING TIBIAL TRAY E1 ANTIOXIDANT INFUSED
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·July 2, 2018
VANGUARD XP TIBIAL LOCKING BAR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBH·July 2, 2018
VANGUARD XP FEMORAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBH·July 2, 2018
BIOMET SERIES A STANDARD PATELLA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·July 2, 2018
XP-XP Tibial Tray - Interlok 65 mm Item # 195752
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·September 18, 2019