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FDA 510(k)

VENT-PLANT DENTAL IMPLANT, OSSEOLOCK AND ROBUTMENT

K-Number: K863755 · 1986-11-07

Decision Date1986-11-07
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VENT-PLANT DENTAL IMPLANT, OSSEOLOCK AND ROBUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Vent-Plant Corporation, Inc.. It received FDA 510(k) clearance on 1986-11-07 under 510(k) number K863755. 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 VENT-PLANT DENTAL IMPLANT, OSSEOLOCK AND ROBUTMENT?

VENT-PLANT DENTAL IMPLANT, OSSEOLOCK AND ROBUTMENT is a medical device that received FDA 510(k) clearance on 1986-11-07. The listed applicant is Vent-Plant Corporation, Inc.. The 510(k) number is K863755.

When did VENT-PLANT DENTAL IMPLANT, OSSEOLOCK AND ROBUTMENT receive FDA 510(k) clearance?

VENT-PLANT DENTAL IMPLANT, OSSEOLOCK AND ROBUTMENT received FDA 510(k) clearance on 1986-11-07, under 510(k) number K863755.

Who is the listed applicant for VENT-PLANT DENTAL IMPLANT, OSSEOLOCK AND ROBUTMENT?

The FDA 510(k) record lists Vent-Plant Corporation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENT-PLANT DENTAL IMPLANT, OSSEOLOCK AND ROBUTMENT?

The FDA product code for VENT-PLANT DENTAL IMPLANT, OSSEOLOCK AND ROBUTMENT 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 Vent-Plant Corporation, 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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