26 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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RUBBERCARE GUARDIAN POLYMER-COATED POWDER-FREE LATEX EXAMINATION GLOVES: CONTAINS 100 MICROGRAMS OR LESS OF TOTAL WATER
FDA 510(k)
FDA Class 1
·General Hospital
Sterling C2000
FDA UDI
SKYTRON LLC·10841736123215·C2000 Standard Rack for Containers
CTXA Hip Bone Mineral Densitometer
FDA UDI
MINDWAYS SOFTWARE, INC.·B052DICTXAHIP0·The CTXA Hip Bone Mineral Densitometer (CTXA Hi...
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00271141·
artVeneer life
FDA UDI
Merz Dental GmbH·D7092002114·artVeneer life upper posteriors, M, C3
BetaForce
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730022035·Beta3 Euro Upper 018 10 archwires per pack
BetaForce™
FDA UDI
Ortho Organizers, Inc.·00190707124441·BETAFORCE Beta³ Euro Upper .018 (10pk)
SCANLAN®
FDA UDI
SCANLAN INTERNATIONAL INC·00846159018103·Dennis Peripheral Vascular Clamp
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112830·BARRON VACUUM PUNCH 9.5MM
3M QUIK TEMP TEMPORIZATION MATERIAL
FDA 510(k)
FDA Class 2
·Dental
RS-4M+MUSCLE STIMULATOR
FDA 510(k)
FDA Class 2
·Physical Medicine
HEYER-SCHULTE BREAST IMPLANT, 150 CC
FDA Adverse Event
V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FTR·May 19, 1994
HEYER-SCHULTE BREAST IMPLANT, 165 CC
FDA Adverse Event
V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FTR·May 19, 1994
3008261720-2024-002114
FDA Adverse Event
Injury
·JJGC INDUSTRIA E COMERCIO DE MATERIAIS DENTARIOS SA·Product code DZE·August 8, 2024
AUTOSOFT XC
FDA Adverse Event
Injury
·UNOMEDICAL UM-D·Product code FPA·January 13, 2025
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·September 14, 2011
TRANS-RAY PLUS 7.5FR 40CC IAB WITH ACCESSORIES
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·April 3, 2024
HEARTSINE SAMARITAN 300P AND PAD PAK
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·February 11, 2013
HIRES 90K
FDA Adverse Event
Malfunction
·ADVANCED BIONICS LLC·Product code MCM·January 31, 2011
ACCU-CHEK AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 20, 2008