902 results · 17ms · Sources: EU EUDAMED, US FDA

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DURA-GUARD PERICARDIUM WITH APEX PROCESSING

FDA Adverse Event
Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code GXQ·May 3, 2013

DURAGEN-UNKNOWN PRODUCT ID

FDA Adverse Event
Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·August 24, 2018

SECURE-C

FDA Adverse Event
Injury ·GLOBUS MEDICAL, INC.·Product code QLQ·March 2, 2026

DISC SHAVER

FDA Adverse Event
Malfunction ·CTL MEDICAL CORPORATION·Product code QLQ·September 29, 2022

SECURE C

FDA Adverse Event
Injury ·GLOBUS MEDICAL, INC.·Product code QLQ·January 14, 2021

ACTIV L INSERTION INSTRUMENT F/H8.5MM

FDA Adverse Event
Injury ·AESCULAP AG·Product code QLQ·March 15, 2022

Manual Instruments Designed For Use With Total Disc Replacement Devices

FDA classification
FDA Class 2 ·Manual Instruments Designed For Use With Total Disc Replacement Devices

NORDENT MANUFACTURING INC

FDA UDI
NORDENT MANUFACTURING INC·00840018614802·CURETTE, DOUBLE END, COLUMBIA 4R-4L QUEENSLAND,...

NORDENT MANUFACTURING INC

FDA UDI
NORDENT MANUFACTURING INC·00840018614772·CURETTE, DOUBLE END, COLUMBIA #2R-2L, QUEENSLAN...

DRIVE SQUARE

FDA UDI
Sin Sistema de Implante Nacional S/A·07899995205315·DRIVE SQUARE

GAMMA CLQ

FDA 510(k)
FDA Class 2 ·Immunology

QNQ Design and Development Pvt. Ltd.

FDA registration
QNQ Design and Development Pvt. Ltd.·4 products·🇮🇳 India

9640 QLT Facebow

FDA UDI
WHIP-MIX CORPORATION·D040343461·A facebow is a device intended for use in a den...

BINDAZYME CLQ CIC EIA KIT

FDA 510(k)
FDA Class 2 ·Immunology

SYSMEX QUICKLYSER-II (QLS-200A)

FDA 510(k)
FDA Class 1 ·Hematology

Facebow with QLT

FDA UDI
WHIP-MIX CORPORATION·D040343441·A facebow is a device intended for use in a den...

QLT ABSOLUTE URINE-HCG PREGNANCY TEST

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

LAS-R HUMAN COMPLEMENT CLQ TEST

FDA 510(k)
FDA Class 2 ·Immunology

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816002780·10,000rpm Mini Centrifuge

Qor Labs

FDA UDI
LW SCIENTIFIC, INC.·00664816003510·10,000rpm Mini 10K Centrifuge