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FDA 510(k)

FLEXIDENT DENTURE

K-Number: K760768 · 1976-10-15

ApplicantFlexodent Corp.
Decision Date1976-10-15
Product CodeEKO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLEXIDENT DENTURE is the device name listed in this FDA 510(k) record. The listed applicant is Flexodent Corp.. It received FDA 510(k) clearance on 1976-10-15 under 510(k) number K760768. The device is classified under product code EKO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIDENT DENTURE?

FLEXIDENT DENTURE is a medical device that received FDA 510(k) clearance on 1976-10-15. The listed applicant is Flexodent Corp.. The 510(k) number is K760768.

When did FLEXIDENT DENTURE receive FDA 510(k) clearance?

FLEXIDENT DENTURE received FDA 510(k) clearance on 1976-10-15, under 510(k) number K760768.

Who is the listed applicant for FLEXIDENT DENTURE?

The FDA 510(k) record lists Flexodent Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEXIDENT DENTURE?

The FDA product code for FLEXIDENT DENTURE is EKO.

Related Clinical Trials

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Related Devices (Code: EKO)

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.

K903672DENE BRIDGEDirotian Pty. , Ltd.K892255DENTAL ROOT ELEVATORZinnanti Surgical Instruments, Inc.K780722ADVANCED DENTURE SYSTEMAdvanced Marketing Research Co.

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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