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Covalon Technologies Inc.

Country not established FDA establishment FEI 3005004019

Site of Covalontechnologies, Inc.

Covalon Technologies Inc. is a medical device manufacturer, with 1 device listed in FDA 510(k) (FDA Unclassified) as of 12 Nov 2026.

Devices
1
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA 510(k) 1
Device classes
  • FDA Unclassified 1
Sites and related companies
Identifiers
  • FDA FEI 3005004019

Catalogue1

Newest first, rows 1-1 of 1

  • ColActive Plus Ref K260652

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

Company details

FDA FEI number
3005004019
Address
1660 TECH AVENUE, MISSISSAUGA Ontario

Frequently asked questions

How many devices does COVALON TECHNOLOGIES INC. have in the registry?

The registry currently lists 1 device for COVALON TECHNOLOGIES INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list COVALON TECHNOLOGIES INC.'s devices?

Among its 1 most recently registered device, COVALON TECHNOLOGIES INC. has devices listed in FDA 510(k) (1 device).

What are the newest devices from COVALON TECHNOLOGIES INC. in the registry?

The most recently registered devices listed for COVALON TECHNOLOGIES INC. include ColActive Plus.

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.