Medical Device Manufacturer · US , Minneapolis , MN

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

10 submissions · 10 cleared · Since 1992

Recent clearances: Stage, STAGE, SPIN-SWI

Total

Cleared

Denied

Spintech, Inc. has 10 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Last cleared in 2022. Active since 1992. Primary specialty: Dental.

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

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

Spintech, 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 - Spintech, Inc.

10 devices

1-10 of 10

SAFETYWAND DISPOSABLE HANDPIECE

K023722 · EJI

Dental · 301d

Cleared Jun 29, 2001

THE WAND PLUS COMPUTER CONTROLLED ANESTHETIC DELIVERY SYSTEM

K010692 · FMF

General Hospital · 113d

Cleared Jun 06, 2000

THE WAND

K992404 · FMF

General Hospital · 323d

SHORTSTOP DISPOSABLE PROPHY ANGLE

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

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

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