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Paco Pharmaceutical Services, Inc.

United StatesFDA applicant, unverified

Devices
13

What Paco Pharmaceutical Services, Inc. makes

Paco Pharmaceutical Services, Inc. manufactures sterile and non-sterile solutions for ocular and contact lens care, including saline solutions, lubricants, disinfectants, and cleaning agents. Their portfolio also includes bandages and preservative-based formulations for contact lens maintenance, such as hydrogen peroxide disinfection solutions and sorbic acid-preserved cleaners.

The company’s products are regulated under FDA classifications, with devices falling into Class I, Class II, and Unclassified (U) categories. These products are authorised via 510(k) clearances and PMA submissions, and the company operates from the United States.

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

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Frequently asked questions

How many devices does Paco Pharmaceutical Services, Inc. have in the registry?

The registry currently lists 13 devices for Paco Pharmaceutical Services, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Paco Pharmaceutical Services, Inc.'s devices?

Among its 13 most recently registered devices, Paco Pharmaceutical Services, Inc. has devices listed in FDA 510(k) (6 devices) and FDA PMA (7 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Paco Pharmaceutical Services, Inc.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for Paco Pharmaceutical Services, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Paco Pharmaceutical Services, Inc. in the registry?

The most recently registered devices listed for Paco Pharmaceutical Services, Inc. include BANDAGE, CHARTER WETTING SOLUTION FOR HARD CONTACT LENSES, STERILE SALINE SOLUTION and CHARTER LABORATORIES INC. LENS LUBRICANT.

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