709 results · 20ms · 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.

DR. GREENSBURG'S HYBRID

FDA 510(k)
FDA Class 2 ·Dental

Marienfeld Superior

FDA UDI
Paul Marienfeld GmbH & Co. KG·04250317339607·

NA

FDA UDI
MAKO SURGICAL CORP.·00848486001339·BONE PINS (4MM X 80MM)

Bernafon

FDA UDI
Bernafon AG·05711584005309·CT7 CPX, VC PS GB CANTEO 7

OsteoMed

FDA UDI
OSTEOMED LLC·00845694052481·1.6mm Twist Drill, 8mm STOP, Hex Shank

Flexitron

FDA UDI
Nucletron B.V.·08717213022140·Flexitron Transfer Tube Set GYN SS

VASOMEDICAL-BIOX 12- CHANNEL AMBULATORY ECG HOLTER RECORDER MODEL 1304, VASOMEDICAL-BIOX 3- CHANNEL MINIATURE AMBULATORY

FDA 510(k)
FDA Class 2 ·Cardiovascular

WELCH ALLYN SPOT VITAL SIGNS LXI MODEL 45000 SERIES

FDA 510(k)
FDA Class 2 ·Cardiovascular

Tandry Locking Plate System

FDA UDI
MICROWARE PRECISION CO., LTD.·04719873098460·2.4mm Locking Volar Distal Radius Plate, 8 Hole...

URETEX SUPPORT PP KIT X1

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION·Product code OTN·April 10, 2013

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·June 2, 2011

ACCU-CHEK COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 13, 2008

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 14, 2026

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026

BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026