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

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2.5mm Insite FT Suture Anchors , 3.5mm Insite FT Suture Anchors

FDA 510(k)
FDA Class 2 ·Orthopedic

Oticon

FDA UDI
Oticon A/S·05707131281616·NERA2, BTE 13 WL 100 TC

Bonding Accessories

FDA UDI
TP ORTHODONTICS INC·00192029000250·Right-On Enamel Cond

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100196·MCINTYRE SPECULUM OPEN WIRE

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100080·TEMPORAL SPECULUM OPEN WIRE

Universal Abutment

FDA UDI
BICON, LLC·00813110021151·Universal Abutment UA5 SP 15° - 2.0mm Post

Scorpio

FDA UDI
Howmedica Osteonics Corp.·07613154020249·Posterior Stabilized Tibial Insert

AUDIT MICROCV HOMOCYSTEINE LINEARITY SET, MODEL 704M-5

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

QUANTA PLEX ANCA PROFILE

FDA 510(k)
FDA Class 2 ·Immunology

BD MULTI-CHECK CD4 LOW CONTROL

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·August 29, 2023

MISAGO RX Self Expanding Peripheral Stem

FDA Enforcement
Class II ·Terminated·Terumo Medical Corp·December 7, 2016

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

STARCLOSE SE VASCULAR CLOSURE SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·June 6, 2013

NI

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code NKB·June 24, 2011

BD MULTI-CHECK CD4 LOW CONTROL

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·August 16, 2023

ROI-C IMPLANT, UNKNOWN SIZE

FDA Adverse Event
Injury ·LDR MÉDICAL·Product code OVE·September 21, 2021

ACE MEDICAL AF W/AS 550 X 1-14ML/HR CPNB

FDA Adverse Event
Injury ·TELEFLEX MEDICAL·Product code MEB·April 6, 2018