Medical Device Manufacturer · US , Walker , MI

Endo Lase, Inc. - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 1984

Total

Cleared

Denied

Endo Lase, Inc. has 24 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 24 cleared submissions from 1984 to 1986.

Browse the FDA 510(k) cleared devices submitted by Endo Lase, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Endo Lase, Inc.

24 devices

1-12 of 24

Cleared Jun 18, 1986

ENDO-LASE CD40 FOR NEUROSURGERY

K853900 · GEX

General & Plastic Surgery · 271d

Cleared May 02, 1986

ENDO-LASE CD-100 CO2 LASER FOR NEUROSURGERY

K853878 · GEX

General & Plastic Surgery · 227d

Cleared Feb 21, 1986

ENDO-LSE CD-100 CO2 LASER FOR GYNECOLOGY

K853876 · HHR

Obstetrics & Gynecology · 157d

Cleared Feb 21, 1986

ENDO-LASE CD40 CO2 FOR GYNECOLOGY

K853903 · HHR

Obstetrics & Gynecology · 154d

Cleared Feb 21, 1986

MEDILAS 2 ND:YAG LASER SURGERY SYSTEM

K855093 · HHR

Obstetrics & Gynecology · 63d

Cleared Feb 19, 1986

ENDO-LASE CD-100 CO2 LASER FOR DERMATOLOGY

K853877 · GEX

General & Plastic Surgery · 155d

Cleared Feb 19, 1986

ENDO-LASE CD 40 FOR DERMATOLOGY

K853901 · GEX

General & Plastic Surgery · 152d

MODEL 700 EVACUATOR FOR USE WITH LASER SURGERY

K860152 · LNK

Gastroenterology & Urology · 21d

Cleared Jan 09, 1986

ENDO-LASE CD-100 CO2 LASER FOR OTORHINOLARYNGOLOGY

K853875 · EWG

Ear, Nose, Throat · 114d

Cleared Jan 09, 1986

ENDO-LASE CD40 FOR OTORHINOLARYNGOLOGY

K853902 · EWG

Ear, Nose, Throat · 111d

Cleared Oct 25, 1985

ENDO-LASE CD-100 CO2 LASER FOR EXTERNAL GENITALIA-

K853874 · GEX

General & Plastic Surgery · 38d

Endo Lase, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Endo Lase, Inc.

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