Medical Device Manufacturer · US , Walker , MI

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

8 submissions · 8 cleared · Since 1981

Recent clearances: FIELD TREND, THE FIELDMASTER MODEL 275, DERMATOLOGY HANDPIECE-OPHTH LASER

View 8 510(k) Devices ↓

Total

Cleared

Denied

Synemed, Inc. has 8 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 8 cleared submissions from 1981 to 1995. Primary specialty: Ophthalmic.

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

Synemed, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

8 devices

1-8 of 8

THE FIELDMASTER MODEL 275

K852936 · HPT

Ophthalmic · 97d

Cleared Dec 03, 1983

DERMATOLOGY HANDPIECE-OPHTH LASER

K833274 · HQF

Ophthalmic · 73d

Cleared Jun 08, 1983

SYNEVAC VACUUM SOURCE UNIT

K831085 · BTA

General & Plastic Surgery · 65d

Cleared Jan 03, 1983

OPTHALAS PHOTOCOAGULATOR

SYNEVAC VACUUM CURETTAGE SYSTEMS

K813282 · HHI

Obstetrics & Gynecology · 27d

Cleared Sep 08, 1981

SCOPE MASTER

K811270 · HIH

Obstetrics & Gynecology · 125d

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

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

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