15 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.

OSSEOFUSE DENTAL IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

ArgenZ HT+ 98x30 ML A1B

FDA UDI
ARGEN CORPORATION, THE·D818131748·Dental porcelain/ceramic restoration kit

Oticon

FDA UDI
Oticon A/S·05707131256720·NERA PRO, RITE 312 WL SIL

VITALCARE STERILEWATER AND 0.9% SODIUM CHLORIDE PRE-FILLED 10CC/30CC SYRINGES

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A

FDA 510(k)
FDA Class 2 ·Cardiovascular

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 16, 2011

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code IOR·October 1, 2014

ROD, FIXATION, INTRAMEDULLARY

FDA Adverse Event
Injury ·SYNTHES USA·Product code HSB·May 4, 2016

ROD, FIXATION, INTRAMEDULLARY

FDA Adverse Event
Injury ·SYNTHES USA·Product code HSB·May 4, 2016

ROD, FIXATION, INTRAMEDULLARY

FDA Adverse Event
Injury ·SYNTHES USA·Product code HSB·May 4, 2016

TFNA FEM NAIL Ø11 R 130° L360 TIMO15

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code HSB·February 23, 2023

FUSION 8MM-40CM UNSUPP PERIPHERAL GRAFT

FDA Adverse Event
Malfunction ·MAQUET CV·Product code DSY·February 8, 2017

ALINITY C MAGNESIUM

FDA Adverse Event
Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code JGJ·February 16, 2026

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 5, 2018