Medical Device Manufacturer · US , Walker , MI

Sharpoint, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1982

Total

Cleared

Denied

Sharpoint, Inc. has 9 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 9 cleared submissions from 1982 to 1986. Primary specialty: Ophthalmic.

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

Sharpoint, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sharpoint, Inc.

9 devices

1-9 of 9

Cleared Oct 24, 1986

COATED SUTURE NEEDLE

K863595 · GAB

General & Plastic Surgery · 39d

Cleared Jun 06, 1986

SURGICAL KNIFE

K861947 · EMF

General & Plastic Surgery · 17d

Cleared May 21, 1984

EAR KNIVES

K840764 · JYO

Ear, Nose, Throat · 88d

Cleared May 09, 1984

CORNEAL SCLERAL LANCE

K840855 · HNN

Ophthalmic · 75d

Cleared Mar 16, 1984

ANTERIOR CAPSULECTOMY CYSTITOME

K840659 · HNY

Ophthalmic · 30d

Cleared Mar 16, 1984

POSTERIOR CAPSULOTOMY CYSTITOME

K840660 · HNY

Ophthalmic · 30d

Cleared Mar 31, 1983

STAINLESS STEEL SUTURE 316L

K830522

General & Plastic Surgery · 42d

Sharpoint, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Sharpoint, Inc.

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