39 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ProLift Lateral HELO Fixated
FDA 510(k)
FDA Class 2
·Orthopedic
NA
FDA UDI
Smith & Nephew, Inc.·03596010101693·STAINLESS STEEL DIVIDERS 196.8MM LONG
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613327520293·ACTIVATION HANDLE
Salvo® Spine System
FDA UDI
Spine Wave, Inc.·10840642174632·9.5 x 60 mm Bone Screw, Cannulated, 3 mm Pitch
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319706213·Boies Nasal Fracture Elevator 7-3/4" (19.4cm)
Vessel Probe 15cm 1.0mm, thin wire red alu handle
FDA UDI
Geister Medizintechnik GmbH·04057034045978·Vessel Probe 15cm 1.0mm, thin wire
red al...
EXPLOR
FDA UDI
Biomet Orthopedics, LLC·00880304210448·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0100610·Caddie Lid, Modular Bone Screws
GLOBAL UNITE
FDA UDI
DEPUY (IRELAND)·10603295430346·GLOBAL UNITE CUTTING GUIDE 128/142 DEGREE
Dilator, Vascular, acc. Geister 15cm 1.0mm alu-handle RED
FDA UDI
Geister Medizintechnik GmbH·04057034045992·Dilator, Vascular, acc. Geister
15cm 1...
DIMENSION CLINICAL CHEMISTRY SYSTEM, MODEL XPAND
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CVM, UNCONJUGATED ESTRIOL (UE3) CALIBRATION VERIFICATION MATERIAL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 5, 2025
EXPLOR 18X24 MM IMPLANT HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWI·July 8, 2020
HEATER/COOLER 3T 110V/60 HZ
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DWC·December 9, 2022
INFUSO.R.
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 12, 2011
CARE ASSIST BED
FDA Adverse Event
Malfunction
·HILL-ROM PLUVIGNER·Product code FNL·June 27, 2013
HS HAND CONTROLLED CURVED SHEA
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code GEI·October 22, 2008
HEATER-COOLER SYSTEM 3T
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DWC·June 4, 2021
EXPLOR 10X22MM IMPLANT HEAD
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code KWI·July 1, 2024