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

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FOUNDATION KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

PILLING

FDA UDI
TELEFLEX INCORPORATED·24026704289428·

Needle Holder

FDA UDI
KOROS U.S.A., INC.·10840199540386·Ryder Needle Holder 21cm 8-1/2"

STAGE IV, AIR-FLUIDIZE BED

FDA 510(k)
FDA Class 2 ·Physical Medicine

ACCLAIM* BRACKET ADHESIVE

FDA 510(k)
FDA Class 2 ·Dental

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

COMPOUNDERS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - BUFFALO GROVE·Product code NEP·October 27, 2012

COMPOUNDERS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - BUFFALO GROVE·Product code NEP·September 6, 2012

COMPOUNDERS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code NEP·August 10, 2012

GOBED II

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·February 15, 2013

MX-PRO AMBULANCE COT

FDA Adverse Event
Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code INK·January 12, 2011

OMNIPOD INSULIN PUMP

FDA Adverse Event
Injury ·INSULET CORPORATION·Product code LZG·July 9, 2014

COMPOUNDERS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - BUFFALO GROVE·Product code NEP·November 2, 2012