OPTI-MAX PRESS-FIT EXTERNAL-HEX DENTAL
K-Number: K944943 · 1995-03-13
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Device Summary
Frequently Asked Questions
What is the OPTI-MAX PRESS-FIT EXTERNAL-HEX DENTAL?
OPTI-MAX PRESS-FIT EXTERNAL-HEX DENTAL is a medical device that received FDA 510(k) clearance on 1995-03-13. The listed applicant is Opti-Max. The 510(k) number is K944943.
When did OPTI-MAX PRESS-FIT EXTERNAL-HEX DENTAL receive FDA 510(k) clearance?
OPTI-MAX PRESS-FIT EXTERNAL-HEX DENTAL received FDA 510(k) clearance on 1995-03-13, under 510(k) number K944943.
Who is the listed applicant for OPTI-MAX PRESS-FIT EXTERNAL-HEX DENTAL?
The FDA 510(k) record lists Opti-Max as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPTI-MAX PRESS-FIT EXTERNAL-HEX DENTAL?
The FDA product code for OPTI-MAX PRESS-FIT EXTERNAL-HEX DENTAL 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 Opti-Max 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.
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