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Shalby Advanced Technologies, Inc.

Also registered as Shalby Advanced Technologies

United Statesfrom the FDA registration address FDA establishment FEI 3020155054

Shalby Advanced Technologies, Inc. is a medical device manufacturer, with 5,023 devices listed as of 12 Nov 2026.

Devices
5,023
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 3,000
  • FDA 510(k) 1

Among the 3,000 best-ranked of 5,023 devices.

Device classes
  • FDA Class II 2,148
  • FDA Class I 792
  • FDA Class III 60

Among the 3,000 best-ranked of 5,023 devices.

Identifiers
  • FDA FEI 3020155054

What Shalby Advanced Technologies, Inc. makes

Shalby Advanced Technologies, Inc. manufactures metallic and polyethylene components for knee and hip arthroplasty, including uncoated knee tibia prostheses, posterior-stabilized total knee prostheses, tibial inserts, and acetabular liners. Their portfolio also includes reusable trial components for knee and acetabular surgeries, as well as bipolar femoral head outer components for hemiarthroplasty. Specific systems include unicompartmental, revision, and total knee replacements, alongside modular hip prostheses.

The company’s devices are classified under FDA categories Class I, Class II, and Class III, with all products listed in the FDA’s Unique Device Identifier (UDI) database. Their products are intended for use in the United States, where regulatory compliance follows FDA requirements for medical devices.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5,023

Newest first, rows 1-50 of 5,023

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Showing 1-50 of 5,023

Company details

FDA FEI number
3020155054
Address
1115 Windfield Way, El Dorado Hills, CA, 95762

Frequently asked questions

How many devices does SHALBY ADVANCED TECHNOLOGIES, INC. have in the registry?

The registry currently lists 5023 devices for SHALBY ADVANCED TECHNOLOGIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list SHALBY ADVANCED TECHNOLOGIES, INC.'s devices?

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

What risk classes do SHALBY ADVANCED TECHNOLOGIES, INC.'s devices fall under?

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

What are the newest devices from SHALBY ADVANCED TECHNOLOGIES, INC. in the registry?

The most recently registered devices listed for SHALBY ADVANCED TECHNOLOGIES, INC. include TaperSet Hip System 1911-3-1105, TaperSet Hip System 1911-3-1075, TaperSet Hip System 1911-3-1135 and TaperSet Hip System 1911-3-1165.

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.