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Hyman, Phelps & McNamara, P.C.

Country not established

Devices
4

What Hyman, Phelps & McNamara, P.C. makes

Hyman, Phelps & McNamara, P.C. manufactures ophthalmic and contact lens care products, including sterile vials for lens solutions, personal lubricant eye drops, and protective cases for contact lenses. Their portfolio also includes lens cleaning and disinfecting systems designed for home use.

These devices are regulated under the FDA’s 510(k) pathway, with classifications ranging from Class I to Class II. The company’s products are listed in the FDA’s 510(k) database, and the firm is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • Menicon Sp Vial Ref K950878

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Comfort Personal Lubricant Ref K915574

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Prophy Pro. Ref K945834

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Pro-Tec-Case Ref K950530

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

Frequently asked questions

How many devices does Hyman, Phelps & McNamara, P.C. have in the registry?

The registry currently lists 4 devices for Hyman, Phelps & McNamara, P.C.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hyman, Phelps & McNamara, P.C.'s devices?

Among its 4 most recently registered devices, Hyman, Phelps & McNamara, P.C. has devices listed in FDA 510(k) (4 devices).

What risk classes do Hyman, Phelps & McNamara, P.C.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for Hyman, Phelps & McNamara, P.C.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Hyman, Phelps & McNamara, P.C. in the registry?

The most recently registered devices listed for Hyman, Phelps & McNamara, P.C. include MENICON SP VIAL, COMFORT PERSONAL LUBRICANT, PROPHY PRO. and PRO-TEC-CASE.

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