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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