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FDA 510(k)

Park Dental Nylon MAD

K-Number: K252976 · 2025-12-18

Decision Date2025-12-18
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Park Dental Nylon MAD is a medical device manufactured by Park Dental Research Corp.. It received FDA 510(k) clearance on 2025-12-18 under approval number K252976. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Park Dental Nylon MAD?

Park Dental Nylon MAD is a medical device that received FDA 510(k) clearance on 2025-12-18. It is manufactured by Park Dental Research Corp.. The 510(k) number is K252976.

When was Park Dental Nylon MAD approved by the FDA?

Park Dental Nylon MAD received FDA 510(k) clearance on 2025-12-18, under approval number K252976.

What company makes Park Dental Nylon MAD?

Park Dental Nylon MAD is manufactured by Park Dental Research Corp..

What is the FDA product code for Park Dental Nylon MAD?

The FDA product code for Park Dental Nylon MAD is LRK.

Related Clinical Trials

Related Devices (Code: LRK)

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.