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FDA 510(k)

SIMDA Abutments

K-Number: K252320 · 2025-12-18

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

Device Summary

SIMDA Abutments is a medical device manufactured by Simda Co., Ltd.. It received FDA 510(k) clearance on 2025-12-18 under approval number K252320. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMDA Abutments?

SIMDA Abutments is a medical device that received FDA 510(k) clearance on 2025-12-18. It is manufactured by Simda Co., Ltd.. The 510(k) number is K252320.

When was SIMDA Abutments approved by the FDA?

SIMDA Abutments received FDA 510(k) clearance on 2025-12-18, under approval number K252320.

What company makes SIMDA Abutments?

SIMDA Abutments is manufactured by Simda Co., Ltd..

What is the FDA product code for SIMDA Abutments?

The FDA product code for SIMDA Abutments is NHA.

Other Devices by Simda Co., Ltd.

Related Devices (Code: NHA)

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.