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Smylio

Also registered as Smylio, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3015143007

Devices
4
Registrations
FDA
FDA recalls
0

Catalogue4

Newest first, rows 1-4 of 4

  • Smylio Aligners Ref K260788

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Nightwear Aligners Ref K221537

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Smylic Invisible Clear Aligners Ref K173784

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Smylio Invisible Clear Aligners Ref K212660

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

Company details

FDA FEI number
3015143007
Address
48890 Milmont Drive, Fremont, CA, 94538

Frequently asked questions

How many devices does SMYLIO have in the registry?

The registry currently lists 4 devices for SMYLIO. Devices recorded under merged duplicate company entries are counted once.

Which registries list SMYLIO's devices?

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

What risk classes do SMYLIO's devices fall under?

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

What are the newest devices from SMYLIO in the registry?

The most recently registered devices listed for SMYLIO include Smylio Aligners, Nightwear Aligners, Smylic Invisible Clear Aligners and Smylio Invisible Clear Aligners.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.