35 results
·
19ms
·
Sources: EU EUDAMED, US FDA
ABCO ULTRA SLIDE MICROSCOPE SLIDE
FDA 510(k)
FDA Class 1
·Pathology
Helix
FDA UDI
Nuvasive, Inc.·00887517134974·Helix R Plate, 32mm 2-Level
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772777648·LUMBAMED BASIC DORSAL STAYS M SILVER II
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950018055·FORCEP WIRE LOOP #23 6" 15CM
Elite Orthopaedics
FDA UDI
Elite Orthopaedics, Inc.·00816591013387·Post Op Telescoping Knee Brace
RAZOR
FDA UDI
Ortho Arch Company Inc·D90980023212·RAZOR JARABAK PLIER
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197418782·Malleable Retractor Blade
51x152...
ZOLL E SERIES 12SL, ANALYSIS OPTION
FDA 510(k)
FDA Class 3
·Cardiovascular
ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS
FDA 510(k)
FDA Class 2
·Orthopedic
HOLDING FORCEPS
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTD·February 16, 2022
SUPERION INDIRECT DECOMPRESSION SYSTEM
FDA Adverse Event
Injury
·VERTIFLEX INC.·Product code NQO·April 3, 2020
VEST MODEL
FDA Adverse Event
Injury
·Product code BYI·April 30, 2014
GOBED II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·October 8, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 31, 2007
Neodent GM X 6mm Engaging Titanium Base, REF: 9007162
FDA Recall
Open, Classified
·Preat Corp·Product code NHA·February 21, 2023
Thermo Fisher Scientific/Microgenics brand CEDIA Tobramycin II Assay, Catalog Number 100018, Product is manufactured and distributed by Microgenics Corporation, located at Fremont, CA., part of Thermo Fisher Scientific The CEDIA Tobramycin II Assay is an in vitro diagnostic medical device intended for the quantitation of Tobramycin in human serum or plasma.
FDA Recall
Terminated
·Microgenics Corp·Product code LFW·October 16, 2013
Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.
FDA Recall
Open, Classified
·Preat Corp·Product code NHA·April 2, 2025
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
FDA Recall
Open, Classified
·Preat Corp·Product code NHA·February 9, 2024
NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662
FDA Recall
Open, Classified
·Preat Corp·Product code NHA·June 25, 2025
Multigent Vancomycin Calibrators; Manufactured by Microgenics Corp, Fremont, CA. Distributed by: Abbott Diagnostics, Abbott Park, IL Product Usage: The Multigent Vancomycin calibrators are intended for use in the calibration of the multiagent vancomycin Vancomycin is a commonly used antibiotic to treat staphylococcus and other gram-positive bacterial infections.
FDA Recall
Terminated
·Microgenics Corp·Product code DLJ·June 8, 2011