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)

LIGHT CURE FILLING MATERIAL

K-Number: K853055 · 1985-11-19

Decision Date1985-11-19
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIGHT CURE FILLING MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Foremost Dental Mfg., Inc.. It received FDA 510(k) clearance on 1985-11-19 under 510(k) number K853055. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT CURE FILLING MATERIAL?

LIGHT CURE FILLING MATERIAL is a medical device that received FDA 510(k) clearance on 1985-11-19. The listed applicant is Foremost Dental Mfg., Inc.. The 510(k) number is K853055.

When did LIGHT CURE FILLING MATERIAL receive FDA 510(k) clearance?

LIGHT CURE FILLING MATERIAL received FDA 510(k) clearance on 1985-11-19, under 510(k) number K853055.

Who is the listed applicant for LIGHT CURE FILLING MATERIAL?

The FDA 510(k) record lists Foremost Dental Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIGHT CURE FILLING MATERIAL?

The FDA product code for LIGHT CURE FILLING MATERIAL is EBF.

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 Foremost Dental Mfg., Inc. 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.

View all 14 devices →

Related Devices (Code: EBF)

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.

↑