22 results · 32ms · 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.

PATRIOT® Lumbar Spacers, SUSTAIN® Spacers

FDA 510(k)
FDA Class 2 ·Orthopedic

Asymmetric Keel Punch Guide Size 3

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215118051·

5MP GRAYSCALE FLAT PANEL DISPLAY, MODEL, 6GF6201-5C$2# (WHERE $ = A-Z AND # = 0-9)

FDA 510(k)
FDA Class 2 ·Radiology

STRAUMANN NARROW NECK CROSSFIT (NNC) 03.3MM DENTAL IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

NEEDLE 18X1-1/2 BLUNT FILL

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code GAA·January 18, 2024

INFUSOR

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 21, 2013

ESTEEM SURGICAL GLOVES

FDA Adverse Event
Injury ·CARDINAL HEALTH·Product code KGO·July 21, 2011

S-ICD SYSTEM

FDA Adverse Event
Injury ·CAMERON HEALTH·Product code LWS·August 7, 2014

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Malfunction ·COOK INC·Product code MMX·March 17, 2022

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Injury ·COOK INC·Product code MMX·September 29, 2021

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Malfunction ·COOK INC·Product code MMX·June 3, 2022

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Malfunction ·COOK INC·Product code MMX·August 15, 2022

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Malfunction ·COOK INC·Product code MMX·January 30, 2023

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Injury ·COOK INC·Product code MMX·February 6, 2023

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Malfunction ·COOK INC·Product code MMX·July 27, 2021

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Malfunction ·COOK INC·Product code MMX·November 4, 2022

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Malfunction ·COOK INC·Product code MMX·March 28, 2022

GUNTHER TULIP VENA CAVA FILTER RETRIEVAL SET

FDA Adverse Event
Injury ·COOK INC·Product code MMX·August 18, 2022

PENUMA IMPLANT

FDA Adverse Event
Injury ·INTERNATIONAL MEDICAL DEVICES, INC.·Product code MIB·October 7, 2019

ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;

FDA Enforcement
Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026