10,000 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GRT LITE, MODEL 8-A
FDA 510(k)
FDA Class 2
·Physical Medicine
Pure Enrichment
FDA UDI
BEAR DOWN CONSULTING·00817387028196·
PILLOW,ECHO WEDGE,GRT GREEN
FDA UDI
Hausmann Enterprises, LLC·00840314807694·
PILLOW,SMALL,12X14X3,GRT GREEN
FDA UDI
Hausmann Enterprises, LLC·00840314807434·
PSN 0 DEG TIB SZ PLT SZ G, RT
FDA UDI
Zimmer, Inc.·00889024705944·
NEXGEN MOLDED CR-FLEX ARTICULAR SURFACE, BLUE, 10 MM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·January 12, 2017
GORE® TAG® CONFORMABLE THORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 4, 2025
NEXGEN PRECOAT STEMMED TIBIAL PLATE SIZE 7
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·January 12, 2017
PERSONA TIBIA 5 SZ G RT- CEMENTED
FDA Adverse Event
Injury
·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code JWH·July 3, 2024
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·August 13, 2024
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·July 17, 2025
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·November 23, 2021
AORTIC EXCLUDER AAA ENDOPROSTHESIS (C3)
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·July 24, 2018
NEXGEN PRECOAT CR-FLEX FEMORAL SIZE G-RT,
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·January 12, 2017
Inion GRT Tack, drill bit and tack appl., 4x, Sterile. Is indicated for the surgical treatment of periodontal defects to aid in the regeneration and integration of tissue components in guided tissue regeneration procedures, for pre-implant and peri-implant surgery and for covering bone defects and empty sockets.
FDA Enforcement
Class II
·Terminated·Inion Ltd.·March 22, 2017
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·November 25, 2021
TB QUANTIFERON GOLD
FDA Adverse Event
Malfunction
·Product code GRT·February 24, 2009
MTD TEST
FDA Adverse Event
Injury
·GEN-PROBE, INC.·Product code GRT·October 25, 1996
TB QUANTIFERON GOLD
FDA Adverse Event
Malfunction
·Product code GRT·February 24, 2009
TB QUANTIFERON GOLD
FDA Adverse Event
Malfunction
·Product code GRT·February 24, 2009