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FDA 510(k)

CURATIVE DENTAL ACRYLIC TEETH

K-Number: K060720 · 2006-08-25

ApplicantCurative, LLC
Decision Date2006-08-25
Product CodeELM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CURATIVE DENTAL ACRYLIC TEETH is the device name listed in this FDA 510(k) record. The listed applicant is Curative, LLC. It received FDA 510(k) clearance on 2006-08-25 under 510(k) number K060720. The device is classified under product code ELM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURATIVE DENTAL ACRYLIC TEETH?

CURATIVE DENTAL ACRYLIC TEETH is a medical device that received FDA 510(k) clearance on 2006-08-25. The listed applicant is Curative, LLC. The 510(k) number is K060720.

When did CURATIVE DENTAL ACRYLIC TEETH receive FDA 510(k) clearance?

CURATIVE DENTAL ACRYLIC TEETH received FDA 510(k) clearance on 2006-08-25, under 510(k) number K060720.

Who is the listed applicant for CURATIVE DENTAL ACRYLIC TEETH?

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

What is the FDA product code for CURATIVE DENTAL ACRYLIC TEETH?

The FDA product code for CURATIVE DENTAL ACRYLIC TEETH is ELM.

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Related Devices (Code: ELM)

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.

K122955DENTAVIT, MONARCH, ACROTONE, SENATOR, DENTORIUMWright Health Group , Ltd.K122925NEW STETIC ARTIFICIAL TEETHNew SteticK122852PHYSIOSTAR NFCCandulor USA, Inc.K121749VERACIAShofu Dental CorporationK120404MERZ DENTAL GMBH ARTEGRAL HD PREFORMED PLASTIC DENTURE TEETHMerz Dental GmbHK120736SR PHONARES IIIvoclar Vivadent, AG

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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