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Can-Am Surgical Corp.

United StatesFDA applicant, unverified

Devices
6

What Can-Am Surgical Corp. makes

Can-Am Surgical Corp. manufactures disposable medical devices including syringes without needles, tuberculin syringes with needles, insulin syringes, and medical lancets.

The company's products are Class II devices listed in the FDA 510(k) registry, and Can-Am Surgical Corp. is based in the US.

AI-generated from registry data, 25 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

  • Disposable Syringe W/O Needle Ref K870190

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Disposable Syringe Tuberculin W/Needle Ref K870192

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Disposable Syringe With Needle Ref K870191

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Amg + Med Lancet Ref K870017

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • E-Z Ject Insulin Syringe Ref K870018

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • A+med Disposable Needle Ref K870193

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

Frequently asked questions

How many devices does Can-Am Surgical Corp. have in the registry?

The registry currently lists 6 devices for Can-Am Surgical Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Can-Am Surgical Corp.'s devices?

Among its 6 most recently registered devices, Can-Am Surgical Corp. has devices listed in FDA 510(k) (6 devices).

What risk classes do Can-Am Surgical Corp.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Can-Am Surgical Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Can-Am Surgical Corp. in the registry?

The most recently registered devices listed for Can-Am Surgical Corp. include DISPOSABLE SYRINGE W/O NEEDLE, DISPOSABLE SYRINGE TUBERCULIN W/NEEDLE, DISPOSABLE SYRINGE WITH NEEDLE and AMG + MED LANCET.

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