37 results · 32ms · Sources: EU EUDAMED, US FDA

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HEBUmedical GmbH

Manufacturer
🇩🇪 Germany

HEBUMEDICAL GMBH

FDA registration
HEBUMEDICAL GMBH·227 products·🇩🇪 Germany

6.5MM RT ANGLE CURETTE

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HTF·November 20, 2025

LEWIN SPINAL PERFORATING FORCEPS

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code GEN·May 11, 2021

LEWIN BONE HOLD CLAMP 7

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code GDJ·November 24, 2017

*

FDA Adverse Event
Other ·HEBUMEDICAL GMBH·Product code LXH·June 26, 2007

*

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code LXT·October 19, 2007

LEWIN BONE HOLDING CLAMP, 7"

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code HXD·March 7, 2007

*

FDA Adverse Event
Other ·HEBUMEDICAL GMBH·Product code HXD·March 27, 2007

HOUSE CURETTES, 7 1/8", DOUBLE-ENDED, 2MM X 2.5MM A

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code JYG·November 7, 2006

*

FDA Adverse Event
Other ·HEBUMEDICAL GMBH·Product code LRW·November 21, 2007

HOUSE CURETTES, 7 1/8", DOUBLE-ENDED, 2MMX2.5MM A

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code FZS·May 3, 2006

LEWIN BONE HOLDING CLAMP, 7"

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code LXH·July 26, 2007

LEWIN BONE HOLDING CLAMP, 7"

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code DXC·June 19, 2008

LEWIN BONE HOLDING CLAMP, 7"

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code HXD·May 30, 2008

LEWIN BONE HOLD CLAMP 7

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code HXD·March 31, 2017

LEWIN BONE HOLD CLAMP 7 / DISCONTINUED-ALT NL6960-1

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code HXD·July 4, 2018

JOSEPH DOUBLE HOOK 5MM

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code GDG·January 19, 2018

VARADY PHLEBECTOMY EXTRACTOR, 6-3/4 SM HOOK

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code GAI·March 14, 2018

MUELLER PHLEB HK RGHT SZ1 4-3/4 IN PHLEBECTOMY HOOK

FDA Adverse Event
Malfunction ·HEBUMEDICAL GMBH·Product code GAI·June 15, 2017