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

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Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen Cannula

FDA 510(k)
FDA Class 2 ·Anesthesiology

ProLift Trial

FDA UDI
Life Spine, Inc.·00190837088385·

PAGODA

FDA Adverse Event
Injury ·ORTHO DEVELOPMENT·Product code NKB·September 21, 2020

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167311515060·

TALOS® HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167321515060·

VACUTRON

FDA UDI
Allied Medical, LLC·00026072004166·MINI-VAC

LUX1540, LUX1440 & LUX2940 LASER HANDPIECES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MIELO-CAN, BEST-LISAS, BEN - BONE BIOPSY. FAST-CUT, COLT, SPRING-CUT, BIO-CUT - SOFT TISSUE BIOPSY

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

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008416·CONTINUOUS INTERMITTENT SUCTION REGULATORS

LUX 1440

FDA Adverse Event
Malfunction ·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008461·CONTINUOUS INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008423·CONTINUOUS INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008454·CONTINUOUS INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008430·CONTINUOUS INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008447·CONTINUOUS INTERMITTENT SUCTION REGULATORS

S3 EX - 3005

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 7, 2013

PARADYM

FDA Adverse Event
Malfunction ·SORIN CRM S.R.L.·Product code MRM·June 24, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 2008

ENDOSKELETON® TCS NO 6 SWIVEL DRIVER

FDA Adverse Event
Malfunction ·TITAN SPINE, LLC·Product code HXX·January 28, 2016

Porex Nostril Retainers, CAT #7241, Size 4, Porex Surgical Inc., 15 Dart Road, Newnan, GA 30265 USA.

FDA Recall
Terminated ·Porex Surgical, Inc.·Product code LYA·July 11, 2006