10,000 results · 96ms · Sources: EU EUDAMED, US FDA

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Spectacle, magnifying

FDA registration
WENZHOU INRAY OPTICAL CO., LTD·1 product·🇨🇳 China

Frame, spectacle

FDA registration
WENZHOU INRAY OPTICAL CO., LTD·1 product·🇨🇳 China

Lens, spectacle, non-custom (prescription)

FDA registration
WENZHOU INRAY OPTICAL CO., LTD·1 product·🇨🇳 China

Sunglasses (non-prescription including photosensitive)

FDA registration
WENZHOU INRAY OPTICAL CO., LTD·1 product·🇨🇳 China

Accu-O-Matic

FDA UDI
ETD Electro-Therapeutic Devices Inc·00628235150057·Advance Transcutaneous Electrical Nerve Stimulator

SafeCross Transseptal RF Puncture and Steerable Balloon Introducer System

FDA UDI
East End Medical I LLC·08600035053013·SafeCross Transseptal RF Puncture and Steerable...

SafeCross Transseptal RF Puncture and Steerable Balloon Introducer System

FDA UDI
East End Medical I LLC·08600035053037·SafeCross Transseptal RF Puncture and Steerable...

SafeCross Transseptal RF Puncture and Steerable Balloon Introducer System

FDA UDI
East End Medical I LLC·08600035053020·SafeCross Transseptal RF Puncture and Steerable...

Saliva, Artificial

FDA Pre-Market Approval
FDA Unclassified ·SALIVART

Signum liquid

FDA registration
KULZER GMBH·2 products·🇩🇪 Germany

Ortho-Choice Ortho-Coat

FDA registration
PULPDENT CORPORATION·2 products·🇺🇸 United States

AGEE-WRISTJACK FRACTURE REACTION SYSTEM (STERILE VERSION), MODEL CFD-147

FDA 510(k)
FDA Class 2 ·Orthopedic

KYPHON® Bone Filler Device (BFD)

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169335868·BONE FILLER DEVICE F04B SIZE 3-RB

KYPHON® Bone Filler Device (BFD)

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000311650·BONE FILLER DEVICE F04B SIZE 3-RB

Salice

FDA registration
SALICE OCCHIALI SRL·1 product·🇮🇹 Italy

Salice

FDA registration
SALICE OCCHIALI SRL·1 product·🇮🇹 Italy

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·AID (R) B/BR HIGH VOLTAGE CABLES FOR ECD SYSTEMS

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·EFH-16; S60-K; S 60-J; S 60-S

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·EFH-16; S 60-K; S 60-J; S 60-S

ClearGuard HD

FDA UDI
Pursuit Vascular, Inc.·B081CGHD106236579·ClearGuard HD end caps are blood access device ...