BELLEGLASS HP MODELING GEL
K-Number: K020178 · 2002-03-15
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Device Summary
Frequently Asked Questions
What is the BELLEGLASS HP MODELING GEL?
BELLEGLASS HP MODELING GEL is a medical device that received FDA 510(k) clearance on 2002-03-15. The listed applicant is Kerr Dental Materials Center. The 510(k) number is K020178.
When did BELLEGLASS HP MODELING GEL receive FDA 510(k) clearance?
BELLEGLASS HP MODELING GEL received FDA 510(k) clearance on 2002-03-15, under 510(k) number K020178.
Who is the listed applicant for BELLEGLASS HP MODELING GEL?
The FDA 510(k) record lists Kerr Dental Materials Center as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BELLEGLASS HP MODELING GEL?
The FDA product code for BELLEGLASS HP MODELING GEL is EBG.
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 Kerr Dental Materials 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: EBG)
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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