25 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HYGEDENT ALGINATE IMPRESSION MATERIAL
FDA 510(k)
FDA Class 2
·Dental
MAXIM KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304008540·
Maxim® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868225222·
GYRUS ACMI, INC
FDA UDI
Gyrus ACMI, LLC·00821925014107·FLPL .6MM PISTON .138"
CAPTURED SCREW ASSEMBLY
FDA UDI
Biomet Orthopedics, LLC·00887868003974·
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036031770·
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776365066·Oral Surgery Suction System
ONEVIEW INTERFACE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)
FDA 510(k)
FDA Class 1
·General Hospital
Widex
FDA UDI
Widex A/S·05706069553833·Widex UNIQUE U-FA (Midnight black ) 440, Teleco...
Widex
FDA UDI
Widex A/S·05706069575811·Widex UNIQUE U-FM (Midnight black ) 440, RC coil
Widex
FDA UDI
Widex A/S·05706069556520·Widex D-FA P (Midnight black ) Dream 440, Telec...
Widex
FDA UDI
Widex A/S·05706069564303·Widex UNIQUE U-FP (Midnight black ) 440, Teleco...
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 4, 2025
MAXIM PRIMARY LIPPED TIBIAL BEARING 12MM X 79/83MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·October 23, 2018
FOOD BOLUS ROTH NET
FDA Adverse Event
Malfunction
·UNITED STATES ENDOSCOPY GROUP, INC.·Product code KOG·May 29, 2013
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·June 25, 2011
LIFEVEST WCD 3000 SYSTEM
FDA Adverse Event
Death
·ZOLL LIFECOR CORPORATION·Product code MVK·August 29, 2008
STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·March 14, 2016
BIOMET ARCOM ALL POLY PAT. BUTTON W/X-RAY WIRE/37 MM (LARGE)
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·October 30, 2017