249 results · 21ms · 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.

HeraBEAT™ US

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

NOVO Surgical

FDA UDI
NOVO SURGICAL, INC.·00842331184246·Cushing Bipolar Forceps, straight, 0.7 mm tip, ...

Orthos

FDA UDI
ORMCO CORPORATION·00889989029901·ORTHOS CM SST ARCH 017X025 LOSM PK10

Symetri Clear

FDA UDI
ORMCO CORPORATION·00889989082890·U1R SYMETRI CLEAR MCLAUGHLIN, BENNETT & TREVISI...

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690198888·AK3 Congruent Insert Trial Size 1, 10mm

CETRA

FDA UDI
Orthofix US LLC·18257200121779·CETRA - IMPLANT/INSTRUMENT TRAY KIT (19-1110)

SPINAL EDGE TITAN PEDICLE SCREW SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

APNEA GUARD

FDA 510(k)
FDA Class 2 ·Dental

EXPERIENCE®

FDA UDI
Gc Orthodontics America Inc.·D78819111000101·EXMRC ROTH 018/UR1 12T 5A

Responsive Orthopedics Total Knee Arthroplasty System

FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973107552·TRIAL 90-SRK-191110 POLY-MPCS 1X10 RIGHT

EXPERIENCE®

FDA UDI
Gc Orthodontics America Inc.·D78819111000201·EXMRC MBT 018/UR1 17T 4A

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025

INFUSOMAT®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 11, 2025

TERUMO CDI 540 CALIBRATOR

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·July 19, 2011

ADVANTAGE SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 26, 2013

TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX

FDA Adverse Event
Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code HCG·September 26, 2008

INFUSOMAT®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 11, 2026

INFUSOMAT®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 7, 2026

INFUSOMAT®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 3, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 5, 2025