20 results · 33ms · Sources: EU EUDAMED, US FDA

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Trulife Inc.

Manufacturer
🇺🇸 United States·5 Importers

TRULIFE, INC.

FDA registration
TRULIFE, INC.·13 products·🇺🇸 United States

TRULIFE, INC.

FDA registration
TRULIFE, INC.·6 products·🇺🇸 United States

LERMAN MINERVA

FDA Adverse Event
Injury ·TRULIFE, INC.·Product code IQF·July 1, 2013

Trulife

Importer
🇮🇪 Ireland·6 Manufacturers

Loth Fabenim B.V.

Importer
🇳🇱 Netherlands·15 Manufacturers

Haltija Group Oy

Importer
🇫🇮 Finland·5 Manufacturers

ORTHO-REHA Neuhof GmbH

Importer
🇩🇪 Germany·17 Manufacturers

Uniprox GmbH & Co.KG

Importer
🇩🇪 Germany·11 Manufacturers

Berner Oy

Importer
🇫🇮 Finland·16 Manufacturers

MDSS GmbH

Authorized representative
🇩🇪 Germany·388 Manufacturers·16562 Devices

630G INSULIN PUMP MMT-1715K 630G BLACK MG

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·April 3, 2023

ENDOWRIST

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·October 29, 2024

DERMABOND PRINEO 42CM MSH 3.8ML ADHESIVE

FDA Adverse Event
Injury ·ETHICON INC.·Product code OMD·November 13, 2025

VCL CT BRD VIO 36IN 1 S/A CTX

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·February 26, 2025

ENDOWRIST

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·October 1, 2024

VCL CT BRD VIO 27IN 2-0 S/A CP-35

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·February 26, 2025

ENDOWRIST

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·October 10, 2024

HAART AORTIC ANNULOPLASTY DEVICE

FDA Adverse Event
Injury ·BIOSTABLE·Product code KRH·June 19, 2024

Caretechion GmbH

Authorized representative
🇩🇪 Germany·158 Manufacturers·1463 Devices