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)

DIPLOMAT

K-Number: K130534 · 2013-10-30

Decision Date2013-10-30
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DIPLOMAT is the device name listed in this FDA 510(k) record. The listed applicant is Diplomat Dental S.R.O.. It received FDA 510(k) clearance on 2013-10-30 under 510(k) number K130534. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIPLOMAT?

DIPLOMAT is a medical device that received FDA 510(k) clearance on 2013-10-30. The listed applicant is Diplomat Dental S.R.O.. The 510(k) number is K130534.

When did DIPLOMAT receive FDA 510(k) clearance?

DIPLOMAT received FDA 510(k) clearance on 2013-10-30, under 510(k) number K130534.

Who is the listed applicant for DIPLOMAT?

The FDA 510(k) record lists Diplomat Dental S.R.O. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIPLOMAT?

The FDA product code for DIPLOMAT is EIA.

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.

Related Devices (Code: EIA)

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.

↑