22 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Model 206 Electrometer/Dosimeter
FDA 510(k)
FDA Class 2
·Radiology
Oticon
FDA UDI
Oticon A/S·05707131286628·RIA2, MINIRITE 312 WL DBL
Nunc IVF ICSI Dish
FDA UDI
Nalge Nunc International Corporation·00866630000410·IVF ICSI DISH
S-LIFT®
FDA UDI
SPINEFRONTIER, INC.·00190361037859·INSERTER, IMPLANT HOLDER, SLAP HAMMER
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690127840·Modular Knee Straight Reamer - 26mm
Temporary Abutment
FDA UDI
BICON, LLC·00813110021045·5.0 x 6.5mm Temporary Abutment - 2.0mm Post
Femoral Trial Size 2N
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215073640·
DIAMOND ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CHRONO-LOG WHOLE BLOOD LUMI-AGGREGOMETER, MODEL 700
FDA 510(k)
FDA Class 2
·Hematology
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·May 26, 2022
T:SLIM G5 SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OYC·December 2, 2021
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 12, 2025
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·June 6, 2013
LIFESTENT FLEXSTAR VASCULAR STENT SYSTEM
FDA Adverse Event
Malfunction
·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code NIP·June 6, 2011
100%SILICONE 2WAY 5CC 16FR
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code KOD·October 14, 2015
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code DQY·December 25, 2016
ROI-C IMPLANT, UNKNOWN SIZE
FDA Adverse Event
Injury
·LDR MÉDICAL·Product code OVE·September 21, 2021
METACROSS RX PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·October 15, 2019