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)

PHOENIX 3.25 MM HA COATED DENTAL IMPLANT

K-Number: K926367 · 1995-09-21

Decision Date1995-09-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PHOENIX 3.25 MM HA COATED DENTAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is International Implant Seminars. It received FDA 510(k) clearance on 1995-09-21 under 510(k) number K926367. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOENIX 3.25 MM HA COATED DENTAL IMPLANT?

PHOENIX 3.25 MM HA COATED DENTAL IMPLANT is a medical device that received FDA 510(k) clearance on 1995-09-21. The listed applicant is International Implant Seminars. The 510(k) number is K926367.

When did PHOENIX 3.25 MM HA COATED DENTAL IMPLANT receive FDA 510(k) clearance?

PHOENIX 3.25 MM HA COATED DENTAL IMPLANT received FDA 510(k) clearance on 1995-09-21, under 510(k) number K926367.

Who is the listed applicant for PHOENIX 3.25 MM HA COATED DENTAL IMPLANT?

The FDA 510(k) record lists International Implant Seminars as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHOENIX 3.25 MM HA COATED DENTAL IMPLANT?

The FDA product code for PHOENIX 3.25 MM HA COATED DENTAL IMPLANT is DZE.

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 International Implant Seminars 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: DZE)

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.

↑