37 results · 20ms · Sources: EU EUDAMED, US FDA

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WATCHHALER

FDA 510(k)
FDA Class 2 ·Anesthesiology

Trumpf Medical

FDA UDI
Baxter Medical Systems GmbH + Co. KG·00887761979390·PST 500

ADC®

FDA UDI
AMERICAN DIAGNOSTIC CORP·00634782002299·Berman Airway, Medium, 80mm,Size 3, 100/cs, Green

n/a

FDA UDI
Ortho Development Corporation·00822409075140·Distal Reamer 10mm

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014600215·D-Series Panel Pad, Right

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702247589·Elvarex 2/Thigh High/Slant-Open Toe/Dotted Sil....

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702399295·Elvarex 2/Knee High/Slant-Closed Toe-Elephantia...

JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955934421·Percutaneous Transluminal Angioplasty Balloon C...

JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955933202·Percutaneous Transluminal Angioplasty Balloon C...

JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955933813·Percutaneous Transluminal Angioplasty Balloon C...

CAMLOG ROOTFORM IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

AVON PATELLO-FEMORAL JOINT PROSTHESIS

FDA 510(k)
FDA Class 2 ·Orthopedic

TRUMPF MEDICAL

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code GDC·December 22, 2025

BD INTIMA-II Y 18GAX1.16IN PRN EC SLM NPVC

FDA Adverse Event
Malfunction ·BD SUZHOU (MDS)·Product code FOZ·April 8, 2024

MetaSystems Probes

FDA UDI
MetaSystems Probes GmbH·04251315818316·XL t(14;18) IGH/BCL2, Dual Fusion Probe

VENTILATION TUBE 7080100 HUNSAKER MON-JE

FDA Adverse Event
Injury ·MEDTRONIC XOMED, INC.·Product code BTR·February 24, 2012

VENTILATION TUBE 7080100 HUNSAKER MON-JE

FDA Adverse Event
Injury ·MEDTRONIC XOMED, INC.·Product code BTR·February 24, 2012

VENTILATION TUBE 7080100 HUNSAKER MON-JE

FDA Adverse Event
Injury ·MEDTRONIC XOMED, INC.·Product code BTR·February 24, 2012

BD INTIMA¿-II Y CLOSED IV CATHETER SYSTEM

FDA Adverse Event
Malfunction ·BD (SUZHOU)·Product code FOZ·August 15, 2023

DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·April 26, 2013