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FDA 510(k)

CUVIS-joint (CJ150)

K-Number: K252037 · 2026-03-25

ApplicantCurexo, Inc.
Decision Date2026-03-25
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CUVIS-joint (CJ150) is a medical device manufactured by Curexo, Inc.. It received FDA 510(k) clearance on 2026-03-25 under approval number K252037. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUVIS-joint (CJ150)?

CUVIS-joint (CJ150) is a medical device that received FDA 510(k) clearance on 2026-03-25. It is manufactured by Curexo, Inc.. The 510(k) number is K252037.

When was CUVIS-joint (CJ150) approved by the FDA?

CUVIS-joint (CJ150) received FDA 510(k) clearance on 2026-03-25, under approval number K252037.

What company makes CUVIS-joint (CJ150)?

CUVIS-joint (CJ150) is manufactured by Curexo, Inc..

What is the FDA product code for CUVIS-joint (CJ150)?

The FDA product code for CUVIS-joint (CJ150) is OLO.

Other Devices by Curexo, Inc.

K201569CUVIS-spine K222698CUVIS-spine K223558CUVIS-spine

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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