18 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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