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Alliance Pharmaceutical Corp.

United StatesFDA applicant, unverified

Devices
2

What Alliance Pharmaceutical Corp. makes

Alliance Pharmaceutical Corp. manufactures SAT PAD™ and SAT PAD, which are designed for the topical administration of medications in medical settings.

These devices are classified as Class II under FDA regulations and are listed in the 510(k) registry. 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

  • Sat Pad(Tm) Ref K926416

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Sat Pad Ref K923948

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

Frequently asked questions

How many devices does Alliance Pharmaceutical Corp. have in the registry?

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

Which registries list Alliance Pharmaceutical Corp.'s devices?

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

What risk classes do Alliance Pharmaceutical Corp.'s devices fall under?

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

What are the newest devices from Alliance Pharmaceutical Corp. in the registry?

The most recently registered devices listed for Alliance Pharmaceutical Corp. include SAT PAD(TM) and SAT PAD.

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