86 results
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19ms
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Sources: EU EUDAMED, US FDA
FOLDING CRUTCH
FDA 510(k)
FDA Class 1
·Physical Medicine
RAZOR
FDA UDI
Ortho Arch Company Inc·D90980023717·RAZOR THREE PRONG PLIER
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197491310·Malleable Retractor Blade, with lip
25x102...
DIALYSATE METER, MODEL D-6
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION
FDA 510(k)
FDA Class 2
·Cardiovascular
SMR GLENOSPHERE Ø 36MM
FDA Adverse Event
Injury
·Product code KWS·June 16, 2021
VRPT PLUS RPF 10MM-15MM TRC W/100MM SLV
FDA Adverse Event
Injury
·COVIDIEN·Product code GCJ·April 30, 2014
SOLETRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MFR·October 22, 2012
FREESTYLE
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code NBW·August 31, 2007
LOGIC CR FEMORAL POR, LEFT, SZ 5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 29, 2023
SMR REVERSE HUMERAL BODY SHORT
FDA Adverse Event
Injury
·LIMACORPORATE SPA·Product code KWS·October 24, 2018
FEMORAL MODULAR HEAD - L Ø28MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LPH·March 18, 2022
Synthes Ti Button Plate 7 Holes, Fastener, Fixation, nondegradable, Soft Tissue
FDA Enforcement
Class II
·Terminated·Synthes (USA) Products LLC·July 13, 2016
***REF LS7600***Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source
FDA Recall
Terminated
·Linvatec Corp. dba ConMed Linvatec·Product code GCT·May 20, 2011
***REF LS7700***Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source
FDA Recall
Terminated
·Linvatec Corp. dba ConMed Linvatec·Product code GCT·May 20, 2011
3M ESPE Unitek Stainless Steel Permanent Molar Crowns , Product Code: 900321, Made in U.S.A by 3M ESPE Dental Products St. Paul, MN 55144-1000.
FDA Recall
Terminated
·Product code ELZ·October 17, 2007
MC5057 12ft/3.6 meters Universal Cable. Made in USA. NON STERILE Rx Only. ConMed Linvatec, 11311 Concept Blvd, Largo, FL 33773. The MC5057 Universal Cable, 12 ft, is used to connect electric handpieces to the power source. The cable is designed with a button feature that allows the user to increase or decrease the operating speed of the handpiece in use. In select handpieces, the cord button feature can select the function, i.e. screw, tap, or drill mode.
FDA Recall
Terminated
·Linvatec Corp. dba ConMed Linvatec·Product code HWE·July 31, 2009
REF IA-2000-S, LightWave Suction Ablator, STERILE, Rx ONLY, MADE IN USA. CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908. ConMed Linvatec LIGHTWAVE SUCTION ABLATOR, electrosurgical cutting and coagulation device and accessories, intended to remove tissue and control bleeding by use of high-frequency electrical current.
FDA Recall
Terminated
·Linvatec Corp. dba ConMed Linvatec·Product code GEI·July 31, 2009
"***All in one CrossFT***Punch***PFT-00M***4.5mm to 6.5mm***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA***" To create pathway for insertion of CrossFT Suture Anchor into bone.
FDA Recall
Terminated
·Linvatec Corp. dba ConMed Linvatec·Product code LXH·April 9, 2012
Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012. A multi position recliner with a steel frame used primarily in clinics, hospitals, and treatment centers for recovery, dialysis, oncology, examination, infusion.
FDA Recall
Terminated
·Winco Mfg., LLC·Product code INM·September 24, 2012