22 results · 24ms · 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.

CAAS Workstation

FDA 510(k)
FDA Class 2 ·Radiology

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100257·CHU ASPIRATING SPECULUM SOLID

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575297931·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575298174·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575298372·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575297238·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575296637·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575297535·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575296514·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575298112·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575297191·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575296835·Knee femur prosthesis trial - General Instrument

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575298297·Knee femur prosthesis trial - General Instrument

JETLITE 5000

FDA 510(k)
FDA Class 2 ·Dental

EVIS EXERA III VIDEO SYSTEM

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

WAVEWRITER ALPHA? 16

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 6, 2024

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·October 8, 2014

UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·July 6, 2011

DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code OJX·June 7, 2013

EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·July 22, 2022