21 results · 21ms · Sources: EU EUDAMED, US FDA

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Imbio Segmentation Editing Tool software

FDA 510(k)
FDA Class 2 ·Radiology

Super Upper Limbs Versalock Plating System

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258663678·VERSALOCK ULNA/RADIUS HOOK PLATE 49.0mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012146·PedFuse Respond, SLD, 8.0mm x 70mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012153·PedFuse Respond, SLD, 8.0mm x 75mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012092·PedFuse Respond, SLD, 8.0mm x 45mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012122·PedFuse Respond, SLD, 8.0mm x 60mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012160·PedFuse Respond, SLD, 8.0mm x 80mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012061·PedFuse Respond, SLD, 8.0mm x 30mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012139·PedFuse Respond, SLD, 8.0mm x 65mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012108·PedFuse Respond, SLD, 8.0mm x 50mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012078·PedFuse Respond, SLD, 8.0mm x 35mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012115·PedFuse Respond, SLD, 8.0mm x 55mm

PedFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361012085·PedFuse Respond, SLD, 8.0mm x 40mm

AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO X

FDA 510(k)
FDA Class 2 ·Cardiovascular

SECURE IMPLANT SYSTEM (2.5/3.0MM)

FDA 510(k)
FDA Class 2 ·Dental

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 24, 2016

LIGAMAX-5MM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 27, 2011

KEEPSAFE FALL MONITOR

FDA Adverse Event
Malfunction ·J. T. POSEY CO.·Product code KMI·June 4, 2013

EVIS EXERA II BRONCHOVIDEOSCOPE

FDA Adverse Event
Injury ·OLYMPUS MED SYSTEMS CORP·Product code EOQ·October 15, 2014

VERSAFITCUP ACETABULAR SHELL CC Ø 56

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·August 12, 2019