510(k) K132956

Device
U FIT DENTAL IMPLANT SYSTEM
Applicant
T STRONG, INC
510(k) number
K132956
Product code
DZE  
Decision
Substantially Equivalent (SESE)
Decision date
2014-06-05
Date received
2013-09-20
Regulation
872.3640
Classification name
Implant, Endosseous, Root-form
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
SUSAN PARK
Address
325 N. Puente St., Unit B Brea CA US 92821 92821

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
08806395270026ABBA-ST Strong Co., Ltd.2026-05-22
08806395270019ABBA-ST Strong Co., Ltd.2026-05-22
08806395270002ABBA-ST Strong Co., Ltd.2026-05-22
08806395269990ABBA-ST Strong Co., Ltd.2026-05-22
08806395269983ABBA-ST Strong Co., Ltd.2026-05-22
08806395269976ABBA-ST Strong Co., Ltd.2026-05-22
08806395269969ABBA-ST Strong Co., Ltd.2026-05-22
08806395269952ABBA-ST Strong Co., Ltd.2026-05-22
08806395269945ABBA-ST Strong Co., Ltd.2026-05-22
08806395269938ABBA-ST Strong Co., Ltd.2026-05-22
08806395269921ABBA-ST Strong Co., Ltd.2026-05-22
08806395269914ABBA-ST Strong Co., Ltd.2026-05-22
08806395269907ABBA-ST Strong Co., Ltd.2026-05-22

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K252145GEN5™ and GEN5+™ 3.3mmD Dental ImplantsParagon Implant Mfg., LLC2025-12-23
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K252090Pterygoid Indication for GM Helix ImplantsJJGC Indústria e Comércio de Materiais Dentários S.A.2025-12-12
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Legacy Summary

summary

FDA Review

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