15 results · 22ms · 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.

STRAUMANN(R) VARIOBASE(TM) ABUTMENT NNC, STRAUMANN(R) VARIOBASE(TM) ABUTMENT RN, STRAUMANN(R) VARIOBASE(TM) ABUTMENT WN,

FDA 510(k)
FDA Class 2 ·Dental

Peerless Buccal Tube

FDA UDI
ORMCO CORPORATION·00889989053630·ORTHOS LSM 6DG -10T B/T NDX LL 22

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613052812·Infusion Handle, Delron, Male To Female Connect...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613069094·Scleral Plug Forceps, Small Cup Shape In The In...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613098148·Infusion Cannula, 20ga, 6mm Tip

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613088057·I/A Handpiece, 17GO, 23GI, 0.3mm, Straight

COMPREHENSIVE LOCKING SCREW

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HWC·July 5, 2019

REVOLUTION SPINAL FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

SOCORRO SMI TUNNEL RELEASE DEVICE

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

S4 IMPLANTS

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code KWP·August 29, 2008

FUJIFILM 600 SERIES ENDOSCOPE EC-600WM

FDA Adverse Event
Malfunction ·FUJIFILM CORPORATION·Product code FDF·January 22, 2025

NAIL HANDLE T2 FEMUR

FDA Adverse Event
Malfunction ·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·May 29, 2013

GORE EXCLUDER AAA ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code MIH·June 14, 2011

VITALITY 2

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 1, 2014

Ultraview SL Command Modules, Model 91496, with the Masimo SpO2 PCBA, PN: 010-1636-02. The Spacelabs Multi-parameter Module is intended for use with the Patient Care Management System (PCMS) to acquire, monitor, and process various clinical parameters from an adult or neonate/infant populations in any type of clinical environment other than home use.

FDA Enforcement
Class II ·Terminated·Spacelabs Healthcare Inc·May 13, 2015