16 results · 22ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

INSIGNIA

FDA 510(k)
FDA Class 2 ·Dental

JOBST UltraSheer

FDA UDI
BSN MEDICAL, INC.·00035664215248·ULTRA SHEER 20-30 MM HG KNEE HIGH CLOSED TOE LA...

TASMIN R 12°

FDA UDI
SIGNUS Medizintechnik GmbH·04047844014981·The basic shape of the TASMIN R devices is a ho...

SafeGuide® Single

FDA UDI
DIVERSATEK HEALTHCARE, INC.·00816734023211·Disposable Over the Guidewire Esophageal Dilato...

Cup Forceps

FDA UDI
ELLIQUENCE, LLC·00846338003548·

MiniSPC Button

FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071152208·12F x 1.5cm MiniSPC Low Profile Suprapubic Cath...

C2000 POWERED WHEELCHAIR

FDA 510(k)
FDA Class 2 ·Physical Medicine

LIGHT CURE DENTAL DAM

FDA 510(k)
FDA Class 1 ·Dental

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 19, 2025

ANGEL SYSTEM WITH ASPIRATION KIT W/ ACDA

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code ORG·March 5, 2019

ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code ORG·May 1, 2019

SIG MOD TIB TRAY CEM COCR 2.5

FDA Adverse Event
Injury ·DEPUY IRELAND ? REG. # 9616671·Product code JWH·May 21, 2013

PALINDROME 19/36 KIT W/ SLOT

FDA Adverse Event
Malfunction ·COSTA RICA·Product code MSD·September 26, 2014

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 13, 2011

MEDTRONIC LEAD

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·September 9, 2020

THINFLAP SYSTEM CROSS-DRIVE, SELF-DRILLING SCREW 1.5X4MM

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code GWO·April 16, 2018