31 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SUPRIS RETROPUBIC SLING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526780811·LEVAMED ACTIVE ANKLE SUP SLVR R III
Vatech Clismile
FDA UDI
Rayence Co., Ltd.·08800018601068·This product is an orthodontic bracket and is u...
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0112330·Tap, 5.50mm, Fixed Sleeve
DANmed
FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351111525·LAP-Instrument, Ø5mm, l=330mm, detach.
Graspi...
DANmed
FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351103766·LAP-Instrument, Ø5mm, l=330mm, detach.
Graspi...
DANmed
FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351114137·LAP-Instrument, Ø5mm, l=330mm, detach.
Graspi...
DANmed
FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351107795·LAP-Instrument, Ø5mm, l=330mm, flushp.
Graspi...
DANmed
FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351101526·LAP-Instrument, Ø5mm, l=330mm, flushp.
Graspi...
DANmed
FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351116346·LAP-Insert only, Ø5mm, l=330mm
Graspi...
DANmed
FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351109676·LAP-Instrument, Ø5mm, l=330mm, detach.
Graspi...
MODIFICATION TO GLUCOSURE BGM SYSTEM, MODEL 221100
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SAFE'N'SOUND PASSIVE DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
PELVILACE BIOURETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·TISSUE SCIENCE LABORATORIES·Product code FTL·May 8, 2013
INDIGO¿
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code HBE·September 23, 2014
CAPSUREFIX NOVUS MRI
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code NVN·June 2, 2011
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 1, 2015
INTROCAN SAFETY® 3
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·November 14, 2025
INTROCAN SAFETY® 3
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·November 12, 2025
INTROCAN SAFETY® 3
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·February 20, 2026