Medical Device Manufacturer · US , Plymouth , MN

Adven Medical

6 submissions · 6 cleared · Since 1994

Total

Cleared

Denied

Adven Medical — FDA 510(k) Submissions

Adven Medical has submitted 6 FDA 510(k) premarket notifications since 1994, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Surgical, Orthopedic, Ac-powered Motor And Accessory/attachment, Sleeve, Limb, Compressible, Trocar, Sinus, Blade, Saw, General & Plastic Surgery, Surgical . Use the specialty filter in the sidebar to narrow results.

6 devices

1–6 of 6

REPROCESSED VENODYNE SEQUENTIAL COMPRESSION SLEEVES / WRAP

K021528 · JOW Sleeve, Limb, Compressible · Cardiovascular

Aug 2002 103d

REPROCESSED DISPOSABLE TROCARS

K013987 · KBG Trocar, Sinus · Ear, Nose, Throat

Mar 2002 87d

REPROCESSED USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS

K012675 · JOW Sleeve, Limb, Compressible · Cardiovascular

Feb 2002 182d

REPROCESSED USED, DISPOSABLE BLADES, BURS, BITS AND TAPS

K012676 · HWE Instrument, Surgical,... · Orthopedic

Feb 2002 174d

REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS

K012694 · HWE Instrument, Surgical,... · Orthopedic

Feb 2002 174d

RE-SHARPENABLE SAW BLADES

K940501 · GFA Blade, Saw, General &... · General & Plastic Surgery

Jun 1994 146d

Adven Medical

Adven Medical — FDA 510(k) Submissions

Filters