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Intl. Medical Industries

United Statesfrom the FDA registration address FDA establishment FEI 1217831

Devices
3
Registrations
FDA
FDA recalls
0

What Intl. Medical Industries makes

International Medical Industries manufactures medical devices including the CHEMO-VENT, a ventilator system for respiratory support, the VERSA-FILL 120 and FILL SET 42-50, which are components for intravenous fluid administration, and tamper-proof caps designed for medication containers to ensure safety and integrity.

The company’s portfolio consists of Class II devices, all of which are listed via the FDA’s 510(k) pathway. These products are regulated under U.S. medical device laws and are based in the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Chemo-Vent Ref K860434

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Versa-Fill 120 & Fill Set 42-50 Ref K850051

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Tamper Proof Cap Ref K861276

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

Company details

FDA FEI number
1217831
Address
2981 Gateway Drive, POMPANO BEACH, FL, 33069

Frequently asked questions

How many devices does INTL. MEDICAL INDUSTRIES have in the registry?

The registry currently lists 3 devices for INTL. MEDICAL INDUSTRIES. Devices recorded under merged duplicate company entries are counted once.

Which registries list INTL. MEDICAL INDUSTRIES's devices?

Among its 3 most recently registered devices, INTL. MEDICAL INDUSTRIES has devices listed in FDA 510(k) (3 devices).

What risk classes do INTL. MEDICAL INDUSTRIES's devices fall under?

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

What are the newest devices from INTL. MEDICAL INDUSTRIES in the registry?

The most recently registered devices listed for INTL. MEDICAL INDUSTRIES include CHEMO-VENT, VERSA-FILL 120 & FILL SET 42-50 and TAMPER PROOF CAP.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.