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Starfish Product Engineering, Inc.

CanadaFDA applicant, unverified FDA

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Starfish Product Engineering, Inc. makes

Starfish Product Engineering, Inc. makes the POD B-SCAN device.

The POD B-SCAN is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.

AI-generated from registry data, 27 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Pod B-Scan Ref K070884

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

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Starfish Product Engineering Toronto Ontario · CA FEI 3020981894

Frequently asked questions

How many devices does Starfish Product Engineering, Inc. have in the registry?

The registry currently lists 1 device for Starfish Product Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Starfish Product Engineering, Inc.'s devices?

Among its 1 most recently registered device, Starfish Product Engineering, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Starfish Product Engineering, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Starfish Product Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Starfish Product Engineering, Inc. in the registry?

The most recently registered devices listed for Starfish Product Engineering, Inc. include POD B-SCAN.

Which FDA establishments are linked to Starfish Product Engineering, Inc.?

1 FDA establishment is linked to Starfish Product Engineering, Inc. in the registry; they are listed on the company page.

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