Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Firstar Dental Handpieces

K-Number: K260029 · 2026-10-01

Decision Date2026-10-01
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Firstar Dental Handpieces is the device name listed in this FDA 510(k) record. The listed applicant is FDC Technology Industry Co.. It received FDA 510(k) clearance on 2026-10-01 under 510(k) number K260029. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Firstar Dental Handpieces?

Firstar Dental Handpieces is a medical device that received FDA 510(k) clearance on 2026-10-01. The listed applicant is FDC Technology Industry Co.. The 510(k) number is K260029.

When did Firstar Dental Handpieces receive FDA 510(k) clearance?

Firstar Dental Handpieces received FDA 510(k) clearance on 2026-10-01, under 510(k) number K260029.

Who is the listed applicant for Firstar Dental Handpieces?

The FDA 510(k) record lists FDC Technology Industry Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Firstar Dental Handpieces?

The FDA product code for Firstar Dental Handpieces is EFB.

Related Clinical Trials

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.

Other records listing FDC Technology Industry Co. 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: EFB)

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

View on FDA Database →

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

↑