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Sutures, Ltd.

United KingdomFDA applicant, unverified

Devices
11

Catalogue11

Newest first, rows 1-11 of 11

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  • Surgibond Ref K943221

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

  • Surgidek Ref K943216

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

  • Plain Catgut Ref K943217

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

  • Surgidek B Ref K943223

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

  • Surgisteel Ref K865038

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

  • Prodek Ref K953609

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

  • Chromic Catgut Ref K943218

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

  • Surgisilk Ref K943627

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

  • Sutulene Ref K943220

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

  • Surgisorb Ref K990432

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

  • Surgidek S Ref K943222

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

Rows 1-11 of 11

Frequently asked questions

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

The registry currently lists 11 devices for Sutures, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sutures, Ltd.'s devices?

Among its 11 most recently registered devices, Sutures, Ltd. has devices listed in FDA 510(k) (11 devices).

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

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

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

The most recently registered devices listed for Sutures, Ltd. include SURGIBOND, SURGIDEK, PLAIN CATGUT and SURGIDEK B.

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