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Albert Browne, Ltd.

Country not established FDA

Devices
61
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Albert Browne, Ltd. makes

Albert Browne, Ltd. manufactures chemical and physical sterilization process indicators, including reusable test strips for validating medical device disinfection solutions. Their product line also includes reusable sterilization indicators for monitoring sterilization cycles, such as those used in autoclaves and other sterilization equipment.

The company’s devices are regulated under FDA Class I and Class II classifications, with submissions recorded in the FDA 510(k) and UDI registries. The portfolio is listed in the United States.

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

Catalogue61

Newest first, rows 1-50 of 61

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  • Verify U504

    Listed Registry: GUDID Class:II
  • VERIFY Bowie Dick

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Verify PCC061

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify RK019

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Verify LCC010

    Listed Registry: GUDID Class:II
  • Verify PCC034

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC029

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC038

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Revital-Ox Resert PCC053

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Verify PCC033

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC006 Open recall

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC007 Open recall

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC003

    Withdrawn Registry: GUDID Class:II
  • Celerity PCC0075

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verdoc RK033

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify RK019

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify LCC028

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • Verify PCC005 Open recall

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Celerity PCC076

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Revital-Ox PCC081

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Celerity PCC079

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Verify PCC037

    Listed Registry: GUDID Class:II
  • Verify LCC016

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC008 Open recall

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC009

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify LCC012

    Listed Registry: GUDID Class:II
  • Celerity PCC0078

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Verify LCC310 Open recall

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC029

    Withdrawn Registry: GUDID Class:II
  • Verify LCC005

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify LCC027

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • Verify LCC016

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC046

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Revital-Ox Resert PCC054

    Withdrawn Registry: GUDID Class:II
  • Verdoc RK028

    Withdrawn Registry: GUDID Class:II
  • Verify LCC016

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Verify PCC048

    Withdrawn Registry: GUDID Class:II
  • Verify PCC031 Open recall

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Celerity PCC074

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Revital-Ox Resert PCC053

    Withdrawn Registry: GUDID Class:II
  • Celerity LCC015

    Active Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID Class:II
  • Revital-Ox Resert PCC054

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Active Regimes: 510(k) Registry: 510(k) Class:II
  • Modified Browne Packaging And Label Steam Process Indicator Ref K032801

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Browne Mvi Steam Indicator Ref K971369

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Active Regimes: 510(k) Registry: 510(k) Class:II
  • Albert Browne Ltd. Verify Steam And Eo Load Record Card Ref K061738

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Browne Ga Indicator For Cidex Products Ref K981054

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Browne Mvi Ethylene Oxide Indicator Ref K991418

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Verify 3-10 Min Flash Integrator Ref K060066

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

Rows 1-50 of 61

Showing 1-50 of 61

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Albert Browne Ltd. LEICESTER · GB FEI 3001168737

Frequently asked questions

How many devices does Albert Browne, Ltd. have in the registry?

The registry currently lists 61 devices for Albert Browne, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Albert Browne, Ltd.'s devices?

Among its 50 most recently registered devices, Albert Browne, Ltd. has devices listed in EUDAMED (9 devices), FDA 510(k) (8 devices) and FDA GUDID (42 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Albert Browne, Ltd.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Albert Browne, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Albert Browne, Ltd. in the registry?

The most recently registered devices listed for Albert Browne, Ltd. include VERIFY U504, VERIFY Bowie Dick, VERIFY PCC061 and VERIFY RK019.

Which FDA establishments are linked to Albert Browne, Ltd.?

1 FDA establishment is linked to Albert Browne, Ltd. in the registry; they are listed on the company page.

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