90 results · 23ms · Sources: EU EUDAMED, US FDA

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FDR D-EVO II FLAT PANEL DETECTOR SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

Equator

FDA UDI
Preat Corporation·00842092186664·Equator Abutment for Astra TX 3.0 x 3mm

PRINCETON

FDA UDI
Princeton Medical Group, Inc.·00810158212107·UTERINE DILATOR HEGAR DOUBLE ENDED 3/4MMØ

OsteoMed

FDA UDI
OSTEOMED LLC·00845694026437·MFx Angulated Locking BSSO Plate, 4 Hole, Short

ELMED

FDA UDI
ELMED INCORPORATED·00842180199613·laminectomy rongeur, CUSHING, 2x10mm, 12.5cm, 4...

LEONE SPA

FDA UDI
LEONE SPA·08033707010876·CALIBRA 1ST MOL BANDS W/G8025-02 n.UR 3

INFINITY TRIDENT NMT POD

FDA 510(k)
FDA Class 2 ·Anesthesiology

XPRESS BALLOON DEVICE

FDA 510(k)
FDA Class 1 ·Ear, Nose, Throat

MITEK, CUFFTACK ANCHOR

FDA Adverse Event
Injury ·MITEK WORLDWIDE·Product code MAI·May 6, 2003

CIRCLE "C" DUAL LUMEN CATHETER KIT

FDA Adverse Event
Malfunction ·HORIZON MEDICAL PRODUCTS, INC.·Product code KOC·February 4, 2003

PERCLOSE

FDA Adverse Event
Other ·PERCLOSE INC·Product code MGB·July 22, 2003

HELICAL BLADE COUPLING SCREW

FDA Adverse Event
Malfunction ·SYNTHES BRANDYWINE·Product code LXH·March 29, 2013

TEMPORARY PACKING WIRE

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code GAO·October 20, 2004

ARTROMOT K3 (KNEE)

FDA Adverse Event
Other ·MEDIREHA GMBH·Product code BXB·June 23, 2003

RITTER

FDA Adverse Event
Malfunction ·MIDMARK CORPORATION·Product code EAZ·January 2, 2026

JOHNSON & JOHNSON ORTHOPAEDICS

FDA Adverse Event
Malfunction ·DEPUY·Product code HWC·January 29, 2003

UNKNOWN SCREWS

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code HWC·September 12, 2019

ARTHROCARE

FDA Adverse Event
Malfunction ·ARTHROCARE CORP.·Product code HRX·November 18, 2003

INTRIGUE13X145MM POLISHED STEM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDG·February 21, 2014

R/B RLOC LHOLE SHL 52MM SZ 23

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·February 21, 2014