39 results · 22ms · Sources: EU EUDAMED, 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