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FDA 510(k)

EVERSTICK PERIO

K-Number: K030072 · 2003-04-10

ApplicantStick Tech , Ltd.
Decision Date2003-04-10
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EVERSTICK PERIO is the device name listed in this FDA 510(k) record. The listed applicant is Stick Tech , Ltd.. It received FDA 510(k) clearance on 2003-04-10 under 510(k) number K030072. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVERSTICK PERIO?

EVERSTICK PERIO is a medical device that received FDA 510(k) clearance on 2003-04-10. The listed applicant is Stick Tech , Ltd.. The 510(k) number is K030072.

When did EVERSTICK PERIO receive FDA 510(k) clearance?

EVERSTICK PERIO received FDA 510(k) clearance on 2003-04-10, under 510(k) number K030072.

Who is the listed applicant for EVERSTICK PERIO?

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

What is the FDA product code for EVERSTICK PERIO?

The FDA product code for EVERSTICK PERIO is EBI.

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 Stick Tech , Ltd. 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.

K051953EVERSTICK A&OK031341STICK FLOWK030820EVERSTICK POSTK021126EVERSTICK ORTHOK011799EVERSTICKNETK011788EVERSTICK

View all 9 devices →

Related Devices (Code: EBI)

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.

K261802Glidewell™ Denture Base ResinPrismatik Dentalcraft, Inc.K261626UltraPrint Flexible Denture UVGuangzhou Heygears IMC., Inc.K262681NanoCeram Resin3BFAB TEKNOLOJI A.S.K262300Denture Base Resin V2Formlabs Ohio, Inc.K261474DENTCA Tru FlexibleDentca, Inc.K260569DB 4000 High Impact Denture BaseCarbon, Inc.

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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