55 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Bright High Flow
FDA 510(k)
FDA Class 2
·Dental
KeyPrint
FDA UDI
Keystone Industries·H66842001551·KeySplint Soft Clear for Carbon 0.5 kg sample
EdgePro
FDA UDI
Biolase, Inc.·00647529004296·A reusable fiberoptic tip accessory intended fo...
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776305307·Richardson Retractor, Lamb Handle, small
Screwdriver
FDA UDI
Treace Medical Concepts, Inc.·00810111222655·Screwdriver
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112908·CORNEAL TREPHINE BLADE7.25MM
ELECSYS ANTI-THYROID PEROXIDASE ANTIBODY TEST SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
DYNA-LOK CLASSIC SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
INTELLIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·July 19, 2018
ST. JUDE
FDA Adverse Event
Injury
·ST. JUDE·Product code DTB·October 11, 2004
PROTECTION SLEEVE FOR FNS INSRT INSTS
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code GEA·July 31, 2024
PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·October 21, 2014
CAPSURE SP NOVUS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 10, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 1, 2013
AEROSET ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING, INC.·Product code JJE·March 11, 2008
AEROSET ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC.·Product code JJE·March 11, 2008
AEROSET ANALYZER
FDA Adverse Event
Other
·ABBOTT MANUFACTURING INC.·Product code JJE·August 7, 2007
PERITX DRAINAGE BAG
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code PNG·April 3, 2026
PERITX PERITONEAL CATHETER & STARTER KIT
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code PNG·October 6, 2025
PERITX PERITONEAL CATHETER & STARTER KIT
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code PNG·October 6, 2025