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Med Science

Also registered as Medscience, Inc.

Country not established

Devices
3
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Med Science makes

Med Science manufactures the ARGIS Pulmonary Function Testing System, a device for assessing lung function metrics, and the Exersystem™ MMC 5000, a motorized medical cycle used for cardiac rehabilitation and exercise testing.

The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. Med Science operates from the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Recap-1 Ref K960641

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Argis Pulmonary Function Testing System Ref K921306

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Exersystem(Tm) Mmc 5000 Ref K864911

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

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 1 recall initiated by Med Science, initiated on 2016-03-22. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2016

    • 22 Mar 2016 Z-1843-2016 Class II Terminated During an FDA inspection it was found that the products are marketed without a cleared 510k. Distribution: Nationwide Distribution to AZ, CA, CO, CT, FL, GA, LA, MD, MI, NJ, NY, PA, TX, VA, and WA.

Frequently asked questions

How many devices does Med Science have in the registry?

The registry currently lists 3 devices for Med Science. Devices recorded under merged duplicate company entries are counted once.

Which registries list Med Science's devices?

Among its 3 most recently registered devices, Med Science has devices listed in FDA 510(k) (3 devices).

What risk classes do Med Science's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Med Science's devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Med Science?

FDA recall records list 1 recall initiated by Med Science, the most recent initiated on 22 Mar 2016. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Med Science in the registry?

The most recently registered devices listed for Med Science include RECAP-1, ARGIS PULMONARY FUNCTION TESTING SYSTEM and EXERSYSTEM(TM) MMC 5000.

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