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Microspecialities, Inc.

Country not established

Devices
215

What Microspecialities, Inc. makes

The company manufactures single-use ophthalmic surgical instruments and accessories, including non-medicated procedure kits, knives, sponges, drapes, lacrimal punctum plugs, vented postsurgical eye shields, and skin marking guides. These products are designed for use in eye surgeries and related procedures, ensuring sterile and precise applications during medical interventions.

The portfolio includes devices classified as Class I, Class II, and unclassified (U) under regulatory frameworks, with several entries listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable domestic and international regulatory standards for medical devices.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue215

Newest first, rows 1-50 of 215

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  • MK8511CB

    Active Regimes: 510(k) Registry: GUDID Class:I
  • MK8510LSK

    Active Regimes: 510(k) Registry: GUDID Class:I
  • 300160

    Active Regimes: 510(k) Registry: GUDID Class:I
  • 300135

    Active Regimes: 510(k) Registry: GUDID Class:I
  • 30020

    Active Regimes: 510(k) Registry: GUDID Class:I
  • MK8507

    Active Regimes: 510(k) Registry: GUDID Class:I
  • MK8508

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Pro-Paks 221018D

    Listed Registry: GUDID Class:II
  • Pro-Paks 467L

    Listed Registry: GUDID Class:II
  • Pro-Paks MK-7630

    Listed Registry: GUDID Class:I
  • Pro-Paks 217312A

    Listed Registry: GUDID Class:II
  • Pro-Paks 267F

    Listed Registry: GUDID Class:II
  • Pro-Paks®️ Mk-110

    Listed Registry: GUDID Class:II
  • Pro-Paks 219042C

    Listed Registry: GUDID Class:II
  • Mk-T102

    Listed Registry: GUDID Class:II
  • Pro-Paks MK-7440

    Listed Registry: GUDID Class:I
  • Pro-Paks MK-7230

    Listed Registry: GUDID Class:I
  • Mk-700700

    Listed Registry: GUDID Class:I
  • Pro-Paks 476E

    Listed Registry: GUDID Class:II
  • Pro-Paks 221122A

    Listed Registry: GUDID Class:II
  • Pro-Paks 220010B

    Listed Registry: GUDID Class:II
  • Pro-Paks 701F

    Listed Registry: GUDID Class:II
  • Comfortear™ 60-6010

    Active Regimes: 510(k) Registry: GUDID Class:—
  • Pro-Paks MK-7305

    Listed Registry: GUDID Class:I
  • Comfortear™ 32-2007

    Active Regimes: 510(k) Registry: GUDID Class:—
  • Pro-Paks 219026B

    Listed Registry: GUDID Class:II
  • Pro-Paks MK-9002

    Listed Registry: GUDID Class:I
  • Pro-Paks®️ Mk-503

    Listed Registry: GUDID Class:II
  • Pro-Paks 218001A

    Listed Registry: GUDID Class:II
  • Mk-700700-40

    Listed Registry: GUDID Class:I
  • Mk-600600-40

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Pro-Paks 701A

    Listed Registry: GUDID Class:II
  • Pro-Paks 21460C

    Listed Registry: GUDID Class:II
  • Mk-100100-20

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Mk-T105

    Listed Registry: GUDID Class:II
  • Pro-Paks 21462B

    Listed Registry: GUDID Class:II
  • Pro-Paks 720C

    Listed Registry: GUDID Class:II
  • Mk-800800+20

    Listed Registry: GUDID Class:I
  • Pro-Paks®️ Mk-108B

    Listed Registry: GUDID Class:II
  • Pro-Paks®️ PD1061

    Listed Registry: GUDID Class:II
  • Mk-100100-10

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Pro-Paks 218036A

    Listed Registry: GUDID Class:II
  • Pro-Paks MK-7435

    Listed Registry: GUDID Class:I
  • Pro-Paks MK-500-6mm

    Listed Registry: GUDID Class:II
  • Mk-100100

    Active Regimes: 510(k) Registry: GUDID Class:I
  • Mk-700700-20

    Listed Registry: GUDID Class:I
  • Pro-Paks 21610C

    Listed Registry: GUDID Class:II
  • Mk-800800

    Listed Registry: GUDID Class:I
  • Pro-Paks 218027C

    Listed Registry: GUDID Class:II
  • Pro-Paks 21410F

    Listed Registry: GUDID Class:II

Rows 1-50 of 215

Showing 1-50 of 215

Company details

DUNS number
013469890
Phone
203-874-1832

Frequently asked questions

How many devices does MICROSPECIALITIES, INC. have in the registry?

The registry currently lists 215 devices for MICROSPECIALITIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list MICROSPECIALITIES, INC.'s devices?

Among its 50 most recently registered devices, MICROSPECIALITIES, INC. has devices listed in FDA GUDID (50 devices).

What risk classes do MICROSPECIALITIES, INC.'s devices fall under?

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

What are the newest devices from MICROSPECIALITIES, INC. in the registry?

The most recently registered devices listed for MICROSPECIALITIES, INC. include MK8511CB, MK8510LSK, 300160 and 300135.

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