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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 the device name listed in this FDA 510(k) record. The listed applicant is Curexo, Inc.. It received FDA 510(k) clearance on 2026-03-25 under 510(k) 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. The listed applicant is Curexo, Inc.. The 510(k) number is K252037.

When did CUVIS-joint (CJ150) receive FDA 510(k) clearance?

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

Who is the listed applicant for CUVIS-joint (CJ150)?

The FDA 510(k) record lists Curexo, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Curexo, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K223558CUVIS-spineK222698CUVIS-spineK201569CUVIS-spine

Related Devices (Code: OLO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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

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