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FDA 510(k)

ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size))

K-Number: K252485 · 2026-04-10

Decision Date2026-04-10
Product CodeOBR
DecisionSubstantially Equivalent

Device Summary

ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size)) is a medical device manufactured by 1987 Media Limited. It received FDA 510(k) clearance on 2026-04-10 under approval number K252485. The device is classified under product code OBR. Product code OBR falls under the category of Orthopedic, which includes orthopedic implants, fixation devices, and surgical instruments. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size))?

ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size)) is a medical device that received FDA 510(k) clearance on 2026-04-10. It is manufactured by 1987 Media Limited. The 510(k) number is K252485.

When was ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size)) approved by the FDA?

ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size)) received FDA 510(k) clearance on 2026-04-10, under approval number K252485.

What company makes ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size))?

ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size)) is manufactured by 1987 Media Limited.

What is the FDA product code for ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size))?

The FDA product code for ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size)) is OBR. This falls under the Orthopedic category.

Related Clinical Trials

Related Devices (Code: OBR)

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.