510(k) K250109

Device
TYBR Collagen Gel
Applicant
Tybr Health
510(k) number
K250109
Product code
OWY
Decision
Substantially Equivalent (SESE)
Decision date
2025-06-06
Date received
2025-01-16
Regulation
878.3300
Classification name
Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Tim Keane
Address
2450 Holcombe Blvd., Suite X Houston TX US 77021 77021

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
00860011716730B3 GEL SystemTybr Health, Inc.2025-12-17

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K212306Tapestry Biointegrative ImplantEmbody, Inc.2021-11-02
K201572TAPESTRY Biointegrative ImplantEmbody, Inc.2020-10-19
K151083BioBridge Collagen MatrixFibralign Corporation2016-01-08
K140300COLLAGEN TENDON SHEET-DDI (CTS-DDI)Rotation Medical, Inc.2014-03-26
K133169MESO TENDON MATRIXKensey Nash Corporation Dba Dsm Biomedical2013-12-20
K131143TRELLIS COLLAGEN RIBBONWrightmedicaltechnologyinc2013-10-07
K120479MTF FASCIAMusculoskeletal Transplant Foundation2012-11-08