17 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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