Medical Device Manufacturer · US , Hopkonton , MA

Endo Surgical Devices, Inc.

2 submissions · 2 cleared · Since 2002

Total

Cleared

Denied

Endo Surgical Devices, Inc. — FDA 510(k) Submissions

Endo Surgical Devices, Inc. has submitted 2 FDA 510(k) premarket notifications since 2002, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Stripper, Artery, Intraluminal . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

CARBODISSECTING ENDOSCOPE

K020925 · DWX Stripper, Artery,... · Cardiovascular

Apr 2003 404d

CARBODISSECTING ENDOSCOPE

K013680 · GEI Electrosurgical, Cutting... · General & Plastic Surgery

Mar 2002 117d

Data Source

FDA 510(k) public files . 174,402 total devices indexed.

Endo Surgical Devices, Inc.

Endo Surgical Devices, Inc. — FDA 510(k) Submissions

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