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Kyocera Medical Technologies, Inc.

Also registered as Kyocera Medical Technologies Inc. (KMTI)

United Statesfrom the FDA registration address FDA establishment FEI 3007932279

Kyocera Medical Technologies, Inc. is a medical device manufacturer, with 7,432 devices listed as of 12 Nov 2026.

Devices
7,432
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 2,999
  • FDA 510(k) 1

Among the 3,000 best-ranked of 7,432 devices.

Device classes
  • FDA Class II 1,604
  • FDA Class I 1,396

Among the 3,000 best-ranked of 7,432 devices.

Identifiers
  • FDA FEI 3007932279

What Kyocera Medical Technologies, Inc. makes

Kyocera Medical Technologies, Inc. manufactures orthopaedic fixation systems, including kits for internal fixation, metallic and polymeric spinal interbody fusion cages, and spinal bone screws made from non-bioabsorbable materials. Their portfolio also includes posterior-stabilized and cruciate-retaining total knee prostheses, as well as unicondylar knee prostheses designed for partial knee replacement.

The company’s devices are regulated under the FDA’s UDI system and fall into Class I and Class II categories. Their products are listed in the FDA’s Unique Device Identification (UDI) database, reflecting compliance with U.S. medical device regulations.

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

Catalogue7,432

Newest first, rows 1-50 of 7,432

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Showing 1-50 of 7,432

Company details

FDA FEI number
3007932279
Address
1289 Bryn Mawr Ave Ste A, Redlands, CA, 92374

Frequently asked questions

How many devices does Kyocera Medical Technologies, Inc. have in the registry?

The registry currently lists 7432 devices for Kyocera Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kyocera Medical Technologies, Inc.'s devices?

Among its 50 most recently registered devices, Kyocera Medical Technologies, Inc. has devices listed in FDA GUDID (50 devices).

What risk classes do Kyocera Medical Technologies, Inc.'s devices fall under?

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

What are the newest devices from Kyocera Medical Technologies, Inc. in the registry?

The most recently registered devices listed for Kyocera Medical Technologies, Inc. include Kyocera Medical Technologies, Inc. Tesera-K XL, Kyocera Medical Technologies, Inc. ALIF and Kyocera Medical Technologies, Inc. Initia T3.

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.