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Puritas Health Care, Inc.

United StatesFDA applicant, unverified

Devices
24

What Puritas Health Care, Inc. makes

Puritas Health Care, Inc. manufactures respiratory and suctioning devices, including oxygen inhaler tubes, tracheal suction catheters, and final filtration systems with extension tubing. Their portfolio also covers silicone clamps and loops, nasal cannulas, sump suction sets with diffuser tips, and measured volume administration sets for intravenous therapy. Additional products include urine meters, stopcocks for IV therapy, and various suction devices with fingertip, funnel, or vacuum-tip attachments.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) clearance registry. These products are intended for use in respiratory support, suctioning, and fluid administration in clinical settings. The manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Puritas Health Care, Inc. have in the registry?

The registry currently lists 24 devices for Puritas Health Care, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Puritas Health Care, Inc.'s devices?

Among its 24 most recently registered devices, Puritas Health Care, Inc. has devices listed in FDA 510(k) (24 devices).

What risk classes do Puritas Health Care, Inc.'s devices fall under?

Among its 24 most recently registered devices, the classes recorded for Puritas Health Care, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Puritas Health Care, Inc. in the registry?

The most recently registered devices listed for Puritas Health Care, Inc. include TUBE, INHALER OXYGEN, TRACHEAL SUCTION CATHETER, 0.22 MICRON FINAL FILTER WITH EXTENSION TUBE and SILCLAMPS DEGANIA SILICONE.

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