40 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.

LaserShot M, NaviLase

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Echo® Bi-Metric® Hip System

FDA UDI
Biomet Orthopedics, LLC·00887868260391·

ECHO BI-METRIC HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304463141·

Bernafon

FDA UDI
Bernafon AG·05711584086827·ZR3, KIT 312 NFM 85 R BE ZERENA 3

OsteoMed

FDA UDI
OSTEOMED LLC·00845694009577·2.0mm x 8mm Cannulated Lag Screw

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668101070·WALTON CONJUNCTIVA RETRACTOR

OsteoMed

FDA UDI
OSTEOMED LLC·00845694070089·Cannulated 2.0 x 8mm Lag Screw Sterile Qty 5

GLIDESHEATH

FDA 510(k)
FDA Class 2 ·Cardiovascular

TOUCHPACS SUITE

FDA 510(k)
FDA Class 2 ·Radiology

ILAB POLARIS MULTI-MODALITY GUIDANCE SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·March 3, 2025

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·April 2, 2019

GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026

ARTICUL/EZE BALL 32 +9 BL

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD·Product code JDI·October 6, 2008

CONTINUUM TRABECULAR METAL SHELL

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code LZO·June 20, 2013

2.7MM/3.5MM LCP LATERAL DISTALFIBULA PLATE 6H/RIGHT/

FDA Adverse Event
Injury ·SYNTHES ELMIRA·Product code HRS·July 28, 2011

PROLENE HERNIA SYSTEM UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTL·April 3, 2019

GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·December 16, 2019

Radius Capspin is a non-sterile instrument for use with other devices in spinal surgery.

FDA Recall
Terminated ·Stryker Spine·Product code LXH·February 19, 2008

Radius Rod Persuader is a non-sterile instrument for use with other devices in spinal surgery.

FDA Recall
Terminated ·Stryker Spine·Product code LXH·February 19, 2008