690 results · 21ms · Sources: EU EUDAMED, US FDA

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STOCKERT COMPACT SYSTEM VERSION 2.0

FDA 510(k)
FDA Class 2 ·Cardiovascular

CTXA Hip Bone Mineral Densitometer

FDA UDI
MINDWAYS SOFTWARE, INC.·B052DICTXAHIP0·The CTXA Hip Bone Mineral Densitometer (CTXA Hi...

artVeneer life

FDA UDI
Merz Dental GmbH·D7092002118·artVeneer life upper posteriors, XS, C3

BetaForce™

FDA UDI
Ortho Organizers, Inc.·00190707124328·Beta Titanium U/L 17x25 (10pk)

BetaForce™

FDA UDI
Ortho Organizers, Inc.·00190707124472·BETAFORCE Beta³ Euro Upper 17x25 (10pk)

BetaForce

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730022066·Beta3 Euro Upper 17x25 10 archwires per pack

BetaForce

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730020178·Beta Titanium U/L 17x25 10 archwires per pack

Metal Custom Rx

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746102431·BRACKET WIDE TWIN 022 TQ=10 A=0 R=0 PROFILE=STD...

Reef TH

FDA UDI
Seaspine Orthopedics Corporation·10889981212834·Trial 11w, 18mm

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150991·Angled Cup Curette Size 6

MODIFICATION TO LIPOPROTEIN (A) SPQ III ANTIBODY REAGENT SET

FDA 510(k)
FDA Class 2 ·Immunology

CORRECT PLUS

FDA 510(k)
FDA Class 2 ·Dental

IMPL TAPERED SP 3.7MM 10M M OCTAGON

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·February 25, 2022

HEARTSINE SAMARITAN 300P AND PAD PAK

FDA Adverse Event
Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·February 11, 2013

SEVEN CONTINUOUS GLUCOSE MONITORING SENSOR

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·February 1, 2011

SOFTCLIX PLUS LANCET DEVICE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·February 20, 2008

IMPL TAPERED SP 3.7MM 8MM OCTAGON

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·January 13, 2022

IMPL TAPERED SP 3.7MM 14M M OCTAGON

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·October 14, 2022

IMPL TAPERED SP 4.8MM 8MM OCTAGON

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·November 17, 2022

OBTAPE TRANSOBTURATOR SLING

FDA Adverse Event
Injury ·MENTOR WORLDWIDE LLC·Product code FTL·October 16, 2012