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

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ICEEDGE 2.4 CRYOABLATION NEEDLE,ICEEDGE 2.4 CRYOABLATION NEEDLE MULTIPACK

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

MAXCUT CARBIDE BUR (10/pk) RASU # 8

FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77811118591·MAXCUT CARBIDE BUR (10/pk) Shape: Round; Size: ...

Flexitron

FDA UDI
Nucletron B.V.·08717213027008·Flexitron Transfer Tube for 4F Flexibles (9)

Plum XLD, list numbers 11859-04-01, 11859-04-03, 11859-04-05, 11859-04-07, 11859-04-09, 11859-04-11, 11859-04-13, 11859-04-51, 12570-04-01 (veterinary); AC cord manufactured by Electri-Cord, Westfield PA, Infusion pumps manufactured by Hospira, Morgan Hill, CA.

FDA Recall
Terminated ·Hospira Inc·Product code FRN·August 11, 2009

KLIMAMED THERMAL MAT & CONTROLLER 95 AND 55 WATTS

FDA 510(k)
FDA Class 2 ·Cardiovascular

REL-K ARTIFICAL LIMB PROSTHESIS

FDA 510(k)
FDA Class 1 ·Physical Medicine

HISTOACRYL BLUE 0.5ML

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code MPN·November 22, 2019

HISTOACRYL BLUE 0.5ML

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code MPN·December 6, 2019

GUARDIAN ROLLING WALKER

FDA Adverse Event
Malfunction ·A&E·Product code ITJ·November 4, 2008

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 14, 2013

ASP AUTOMATIC ENDOSCOPE REPROCESSOR WITH PRINTER

FDA Adverse Event
Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code FEB·August 13, 2008

HISTOACRYL BLUE 0.5ML

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code MPN·June 27, 2019

HISTOACRYL BLUE 0.5ML

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code MPN·October 17, 2019

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 8, 2025

BioMend¿ Extend" Absorbable Collagen Membrane BioMend¿ Extend" Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corporation·May 22, 2013

IMP,TSV,MCOL MG,4.7MM,10M

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·May 21, 2024

IMP,TSV,MCOL MG,4.7MM,11.5MML

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·May 21, 2024

IMP,TSV,MCOL MG,4.7MM,11.5MML

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·June 12, 2024

IMP,TSV,MCOL MG,3.7MM,11.5MML

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·July 23, 2024

IMP,TSV,MCOL MG,4.7MM,11.5MML

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·August 1, 2023