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FDA 510(k)

R & S SERIES IMPLANTS

K-Number: K811923 · 1981-07-24

ApplicantSuncoast Dental Corp.
Decision Date1981-07-24
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

R & S SERIES IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Suncoast Dental Corp.. It received FDA 510(k) clearance on 1981-07-24 under 510(k) number K811923. 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 R & S SERIES IMPLANTS?

R & S SERIES IMPLANTS is a medical device that received FDA 510(k) clearance on 1981-07-24. The listed applicant is Suncoast Dental Corp.. The 510(k) number is K811923.

When did R & S SERIES IMPLANTS receive FDA 510(k) clearance?

R & S SERIES IMPLANTS received FDA 510(k) clearance on 1981-07-24, under 510(k) number K811923.

Who is the listed applicant for R & S SERIES IMPLANTS?

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

What is the FDA product code for R & S SERIES IMPLANTS?

The FDA product code for R & S SERIES IMPLANTS 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.

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Other records listing Suncoast Dental Corp. 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.

K811889R & S SERIES FITTING TOOLS

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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