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Spintech, Inc.

Also registered as Spintech, LLC

United StatesFDA applicant, unverified FDA FEI 3020162557

Spintech, Inc. is a medical device manufacturer, with 16 devices listed in FDA 510(k) and FDA GUDID (FDA Class II and I) as of 13 Nov 2026.

Devices
16
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA 510(k) 12
  • FDA GUDID 4

A device listed in two registries counts in both.

Device classes
  • FDA Class II 15
  • FDA Class I 1
Identifiers
  • FDA FEI 3020162557
  • DUNS 105125594

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue16

Newest first, rows 1-16 of 16

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  • Stage 2.4

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Stage 1.1

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Stage 2

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Stage 2.3

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Wand Plus Ref K992819

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Leaplaza Frame Ref K922238

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Spin Care Disposable Protective Mask Level 3 Ref K212109

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Safetywand Disposable Handpiece Ref K023722

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Spin-Swi Ref K173224

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Stage Ref K223079

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • The Wand Plus Computer Controlled Anesthetic Delivery System Ref K010692

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Spin Care Disposable Protective Mask Ref K201624

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • The Wand Ref K992404

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • The Wand Ref K961648

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Stage Ref K210843

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Shortstop Disposable Prophy Angle Ref K955654

    Active Regimes: 510(k) Registry: 510(k) Class:I

Rows 1-16 of 16

Company details

FDA FEI number
3020162557
DUNS number
105125594
Address
30200 Telegraph Road, Bingham Farms, MI, 48025
Phone
+2487126789

Frequently asked questions

How many devices does Spintech, Inc. have in the registry?

The registry currently lists 16 devices for Spintech, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Spintech, Inc.'s devices?

Among its 16 most recently registered devices, Spintech, Inc. has devices listed in FDA 510(k) (12 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Spintech, Inc.'s devices fall under?

Among its 16 most recently registered devices, the classes recorded for Spintech, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Spintech, Inc. in the registry?

The most recently registered devices listed for Spintech, Inc. include STAGE 2.4, STAGE 1.1, STAGE 2 and STAGE 2.3.

Generated automatically from registry data and not verified by a human reviewer.