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FDA 510(k)

SIMDA abutment

K-Number: K232271 · 2023-10-26

Decision Date2023-10-26
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SIMDA abutment is the device name listed in this FDA 510(k) record. The listed applicant is Simda Co., Ltd.. It received FDA 510(k) clearance on 2023-10-26 under 510(k) number K232271. 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 abutment?

SIMDA abutment is a medical device that received FDA 510(k) clearance on 2023-10-26. The listed applicant is Simda Co., Ltd.. The 510(k) number is K232271.

When did SIMDA abutment receive FDA 510(k) clearance?

SIMDA abutment received FDA 510(k) clearance on 2023-10-26, under 510(k) number K232271.

Who is the listed applicant for SIMDA abutment?

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

What is the FDA product code for SIMDA abutment?

The FDA product code for SIMDA abutment is NHA.

Other records listing Simda Co., Ltd. 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.

Related Devices (Code: NHA)

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.

Official Source

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