36 results · 23ms · Sources: EU EUDAMED, US FDA

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MARROWMINER

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

DHF 0.2 HEMOCONCENTRATOR: DIDECO NEWBORN-INFANT HEMONCENTRATION; DHR 0.6 HEMOCONCENTRATOR: DIDECO PEDIATRIC/SMALL ADULT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

EBI ACUMEN SURGICAL NAVIGATION SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·April 22, 2013

ENDOPATH STEALTH CIR STAPLER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code KOG·April 28, 2011

RESTORE ADVANCED RECHARGEABLE

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·July 9, 2008

REVITAN, PROXIMAL PART, CONICAL, UNCEMENTED, 75, TAPER 12/14

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LZO·April 26, 2019

REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/260

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·May 6, 2019

REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 18/140

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·April 29, 2019

REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 26/260

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·April 26, 2019

REVITAN, PROXIMAL PART, CYLINDRICAL, UNCEMENTED, 65, TAPER 12/14

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·April 29, 2019

DHF 06 HEMOCONCENTRATOR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALY·Product code KDI·May 22, 2025

REVITAN, DISTAL PART, CURVED, UNCEMENTED, 20/200

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code KWA·February 13, 2019

REVITAN, DISTAL PART, STRAIGHT, UNCEMENTED, 20/140

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·August 7, 2018

OPTAN, STEM, RIGHT, UNCEMENTED, 16, TAPER 12/14

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code LZO·June 4, 2018

TOSOH HLC-723G8 ANALYZER

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

TOSOH HLC-723G8 ANALYZER

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·December 15, 2017

TOSOH HLC-723G8 ANALYZER

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

TOSOH HLC-723G8 ANALYZER

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code LCP·December 11, 2017

REVITAN DIST. CURVED 16/200

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·October 5, 2018