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 4.0 MM ANGLED DENTAL ATTACHMENTS

K-Number: K926311 · 1995-09-21

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

Device Summary

PHOENIX 4.0 MM ANGLED DENTAL ATTACHMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Vancouver Implant Center. It received FDA 510(k) clearance on 1995-09-21 under 510(k) number K926311. 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 4.0 MM ANGLED DENTAL ATTACHMENTS?

PHOENIX 4.0 MM ANGLED DENTAL ATTACHMENTS is a medical device that received FDA 510(k) clearance on 1995-09-21. The listed applicant is Vancouver Implant Center. The 510(k) number is K926311.

When did PHOENIX 4.0 MM ANGLED DENTAL ATTACHMENTS receive FDA 510(k) clearance?

PHOENIX 4.0 MM ANGLED DENTAL ATTACHMENTS received FDA 510(k) clearance on 1995-09-21, under 510(k) number K926311.

Who is the listed applicant for PHOENIX 4.0 MM ANGLED DENTAL ATTACHMENTS?

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

What is the FDA product code for PHOENIX 4.0 MM ANGLED DENTAL ATTACHMENTS?

The FDA product code for PHOENIX 4.0 MM ANGLED DENTAL ATTACHMENTS 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 Vancouver Implant Center 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.

↑