18 results · 19ms · Sources: EU EUDAMED, US FDA

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SONIC SCALER WITH FIBER OPTIC, MODEL NAS-L, SONIC SCALER WITHOUT FIBER OPTIC, MODEL NAS-NL

FDA 510(k)
FDA Class 2 ·Dental

SCOTT'S BENT NEEDLE TIPS (100) YELLOW 20 G

FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77819910211·SCOTT'S BENT NEEDLE TIPS (100) YELLOW 20 G

Zavation

FDA UDI
Zavation LLC·00842166118300·Posterior Cervical Depth Guage

MODIFICATION TO MEDICOMPASS CONNECT

FDA 510(k)
FDA Class 2 ·Cardiovascular

Terragene Bionova, Terragene Bionova, Terragene Integron, Terragene Cintape, Terragene Chemdye

FDA 510(k)
FDA Class 2 ·General Hospital

ZMR®

FDA UDI
Zimmer, Inc.·00889024162006·

ZMR®

FDA UDI
Zimmer, Inc.·00889024162013·

COLORADO 2 SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MNH·December 4, 2009

SPINNING SPIROS CLOSED MALE LUER, RED CAP

FDA Adverse Event
Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·January 7, 2021

SPINNING SPIROS CLOSED MALE LUER, RED CAP

FDA Adverse Event
Malfunction ·ICU MEDICAL INC·Product code FPA·December 3, 2020

COLORADO II SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code MNH·May 19, 2017

COLORADO SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·October 17, 2016

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·ANIMAS CORPORATION·Product code LZG·March 6, 2013

LANX SPINAL FIXATION SYSTEM

FDA Adverse Event
Injury ·LANX, LLC·Product code NKB·February 11, 2011

CAPSURE Z NOVUS

FDA Adverse Event
Injury ·MPRI·Product code DTB·August 8, 2014

COLORADO II SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·July 26, 2011

METRX SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·June 10, 2024

Zimmer ZMR Femoral Spout & Cone Bodies and Trabecular Metal Hip Prosthesis Femoral Stems: FEMORAL BODY REVISION NITRIDED POROUS 12/14 NECK TAPER EXTENDED 46 MM NECK OFFSET SPOUT BODY SIZE E 55 MM BUILD-UP TIVANIUM TI-6AL-4V ALLOY STERILE. Item number: 00-9991-021-55

FDA Recall
Terminated ·Zimmer Inc.·Product code LPH·November 16, 2011