Skip to content

Interpro Intl., Inc.

United StatesFDA applicant, unverified

Devices
11

What Interpro Intl., Inc. makes

Interpro Intl., Inc. manufactures single-use patient examination gloves (latex and vinyl), surgical gloves, isolation gowns, surgical caps, laparotomy sponges, gauze sponges, and shoe covers. These items are designed for medical, surgical, and examination settings to maintain hygiene and barrier protection during procedures.

The company’s products are regulated under FDA Class I and Class II designations, with some devices classified as unclassified (U). These items are listed via the FDA’s 510(k) pathway, and the manufacturer is based in the United States.

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

Catalogue11

Newest first, rows 1-11 of 11

Search and filter all 11 devices
Skip device list

  • Patient Examination Gloves (Latex) Ref K891438

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

  • Patient Examination Gloves (Latex) Ref K891642

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

  • Vinyl Examination Gloves (Mfg. Salzgitter Morex) Ref K890968

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

  • Interpro Int'l, Inc. Isolation Gown Ref K874766

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

  • Latex Examination Gloves (Mfg. Ningbo Medical) Ref K890891

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

  • Patient Examination Gloves (Latex) Ref K891440

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

  • Laparotomy Sponges Ref K874065

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

  • Surgical Caps Ref K874066

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

  • Guaze Sponges Ref K874067

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

  • Shoe Covers Ref K874064

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

  • Surgeons Gloves Ref K881374

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

Rows 1-11 of 11

Frequently asked questions

How many devices does Interpro Intl., Inc. have in the registry?

The registry currently lists 11 devices for Interpro Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Interpro Intl., Inc.'s devices?

Among its 11 most recently registered devices, Interpro Intl., Inc. has devices listed in FDA 510(k) (11 devices).

What risk classes do Interpro Intl., Inc.'s devices fall under?

Among its 11 most recently registered devices, the classes recorded for Interpro Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Interpro Intl., Inc. in the registry?

The most recently registered devices listed for Interpro Intl., Inc. include PATIENT EXAMINATION GLOVES (LATEX), VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX), INTERPRO INT'L, INC. ISOLATION GOWN and LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL).

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