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Clinitex Medical Corp.

United StatesFDA applicant, unverified

Devices
2

What Clinitex Medical Corp. makes

Clinitex Medical Corp. manufactures CLINITEX CAST PADDING, a protective material used to cushion and support immobilised limbs during fracture healing, and CLINITEX STOCKINETTE, a compression stockinette for post-surgical or post-injury limb coverage and circulation support.

These products are Class I medical devices regulated under the FDA’s 510(k) pathway, and the company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Clinitex Cast Padding Ref K973420

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Clinitex Stockinette Ref K973417

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

Frequently asked questions

How many devices does Clinitex Medical Corp. have in the registry?

The registry currently lists 2 devices for Clinitex Medical Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Clinitex Medical Corp.'s devices?

Among its 2 most recently registered devices, Clinitex Medical Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Clinitex Medical Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Clinitex Medical Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Clinitex Medical Corp. in the registry?

The most recently registered devices listed for Clinitex Medical Corp. include CLINITEX CAST PADDING and CLINITEX STOCKINETTE.

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