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Sialo Technology, Ltd.

IsraelFDA applicant, unverified

Devices
4

Catalogue4

Newest first, rows 1-4 of 4

  • Sialo Balloon Dilatation Catheter Ref K072749

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Sialo Drain Ref K072334

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Stone Grasping Basket, Model Pd-T1 2115 Ref K082735

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Modular Endoscope Ref K093785

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

Frequently asked questions

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

The registry currently lists 4 devices for Sialo Technology, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sialo Technology, Ltd.'s devices?

Among its 4 most recently registered devices, Sialo Technology, Ltd. has devices listed in FDA 510(k) (4 devices).

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

Among its 4 most recently registered devices, the classes recorded for Sialo Technology, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Sialo Technology, Ltd. include SIALO BALLOON DILATATION CATHETER, SIALO DRAIN, STONE GRASPING BASKET, MODEL PD-T1 2115 and MODULAR ENDOSCOPE.

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