20 results
·
21ms
·
Sources: EU EUDAMED, US FDA
THERMO SCIENTIFIC QMS EVEROLIMUS REAGENTS, CALIBRATORS AND CONTROLS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Duette™
FDA UDI
POIESIS MEDICAL, LLC·10852732004088·14FR Duette™ Indwelling Urinary Catheter Urine ...
Vilex Guidewire
FDA UDI
VILEX IN TENNESSEE, INC.·00841731120342·Guidewire 1.4x100mm Sgl Trocar
OsteoMed
FDA UDI
OSTEOMED LLC·00845694025843·Genio Plate, 8mm, Rigid
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450172506·
LINER #L FOR MOBILE LINER Ø42
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LZO·January 5, 2022
FIREBIRD SPINAL FIXATION SYSTEM, FIREBIRD SIDE-LOADING BODY
FDA 510(k)
FDA Class 2
·Orthopedic
NIPRO INSULIN SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
Widex
FDA UDI
Widex A/S·05706069664058·Widex UNIQUE U-PA 440 DEMO (Winter silver ) RC ...
EQUINOXE CAGE GLENOID SMALL, ALPHA
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWS·August 1, 2023
MAINFRAME 8253001 NIM RESPONSE 3.0
FDA Adverse Event
Injury
·MEDTRONIC XOMED, INC.·Product code ETN·May 8, 2013
TERUMO CERTRIFUGAL SYSTEM
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWA·May 16, 2011
SAGB QUICK CLOSE
FDA Adverse Event
Malfunction
·OBTECH MEDICAL SARL·Product code LTI·August 5, 2008
SMR HUMERAL HEAD Ø48 MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWT·May 8, 2024
COBALT¿ XT HF QUAD CRT-D MRI SURESCAN¿
FDA Adverse Event
Malfunction
·MEDTRONIC EUROPE SARL·Product code NIK·August 11, 2023
ATTAIN ABILITY MRI SURESCAN
FDA Adverse Event
Injury
·MPRI·Product code OJX·February 26, 2024
SMR REVERSE FINNED HUMER. BODY
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A·Product code PHX·June 14, 2023
E-Z WIDER BARIATRIC CHAIR BED; Single Motion Expandable Width Technology
FDA Enforcement
Class II
·Terminated·Kreg Medical Inc.·June 12, 2013
CME America T-Syringe Pump - T34 - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous, intra-arterial, epidural, in close proximity to nerves, and into an intra-operative site (soft tissue/body cavity/surgical wound site).
FDA Enforcement
Class II
·Terminated·CME America, LLC·December 9, 2020
1202 Flex Focus Ultrasound System, cart models UA1214 and UA1814, used with: Flex Focus 200, Flex Focus 300, Flex Focus 400, Flex Focus 500, Flex Focus 700, Flex Focus 800; System, Imaging, Pulsed Doppler, Ultrasonic
FDA Enforcement
Class II
·Ongoing·B-K Medical A/S·November 12, 2025