146 results · 20ms · Sources: EU EUDAMED, US FDA

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Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 2 ·AccelStimTM Bone Growth Stimulator

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 2 ·AccelStim™

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 2 ·AccelStim

APEX Spine System

FDA UDI
SPINECRAFT, LLC·00193082014772·APEX Ti Poly Screw Dia.10.0, 35mm

APEX Spine System

FDA UDI
SPINECRAFT, LLC·M824P6100351·Polyaxial Pedicle Screw, 10.0mm x 35mm

Direct Plastic Cylinder With Hex.

FDA UDI
NOGA MEDICAL PRODUCTS LTD·07290118141570·Direct Plastic Cylinder With Hex.

esthetic

FDA UDI
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011086·

Restore

FDA UDI
KEYSTONE DENTAL, INC.·D768L21003519K0·Hex Driver

NA

FDA UDI
Biedermann Motech GmbH & Co. KG·04250869604048·MOSS Ti Rod, Ø5.5x35mm curved

APEX Spine System

FDA UDI
SPINECRAFT, LLC·M824SCP6100351·Polyaxial Pedicle Screw, 10.0 x 35mm

NA

FDA UDI
Biedermann Motech GmbH & Co. KG·04250869609111·MOSS VRS Ti rod, Ø5.5x35mm, curved

Restore

FDA UDI
KEYSTONE DENTAL, INC.·D768L21003524K0·Hex Driver

ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System, MegaCerfix Anterior Cervical Plate System, Spinema Lumbar Plate System

FDA 510(k)
FDA Class 2 ·Orthopedic

CASPER X

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 11, 2025

CASPER 5F

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 24, 2025

Stent, Iliac

FDA Pre-Market Approval
FDA Class 3 ·EPIC SELF-EXPANDING NITINOL STENT SYSTEM

Normothermic Machine Perfusion System For The Preservation Of Donor Livers Prior To Transplantation

FDA Pre-Market Approval
FDA Class 3 ·OrganOx metra System

DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM DEXCOM SHARE SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·May 16, 2016

VRPT PLUS RPF 10MM-15MM TRC W/100MM SLV

FDA Adverse Event
Malfunction ·PONCE-USS·Product code GCJ·October 21, 2008

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code NKB·August 12, 2011