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FDA 510(k)

VIVADENT FILPIN

K-Number: K863831 · 1986-10-14

ApplicantVivadent (Usa), Inc.
Decision Date1986-10-14
Product CodeEBL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VIVADENT FILPIN is the device name listed in this FDA 510(k) record. The listed applicant is Vivadent (Usa), Inc.. It received FDA 510(k) clearance on 1986-10-14 under 510(k) number K863831. The device is classified under product code EBL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIVADENT FILPIN?

VIVADENT FILPIN is a medical device that received FDA 510(k) clearance on 1986-10-14. The listed applicant is Vivadent (Usa), Inc.. The 510(k) number is K863831.

When did VIVADENT FILPIN receive FDA 510(k) clearance?

VIVADENT FILPIN received FDA 510(k) clearance on 1986-10-14, under 510(k) number K863831.

Who is the listed applicant for VIVADENT FILPIN?

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

What is the FDA product code for VIVADENT FILPIN?

The FDA product code for VIVADENT FILPIN is EBL.

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Other records listing Vivadent (Usa), 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.

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Related Devices (Code: EBL)

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.

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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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