Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3032412536

FEI Number

3032412536

Entity Name

THERAMICRO

City/State/Country

Cordova, TN, US

Establishment Address

51 Germantown Ct Ste 200, Cordova, TN 38018, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Theramicro (Owner Number: 10093892)

Owner / Operator Contact Address

51 Germantown Court, Suite 200, Cordova, TN 38018, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K251063

PMA Number

N/A

All Registered Proprietary Names

TeKForce Knotless Syndesmosis Implant TekBrace TeKForce All Suture Anchor TekBrace Solo Soft Tissue Reinforcement Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HTN	Washer, Bolt Nut	Orthopedic	Class 2	888.3030	2026-04-13
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2025-07-30
MBI	Fastener, Fixation, Nondegradable, Soft Tissue	Orthopedic	Class 2	888.3040	2026-04-13
FTL	Mesh, Surgical, Polymeric	General, Plastic Surgery	Class 2	878.3300	2025-07-30
OWX	Mesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon	General, Plastic Surgery	Class 2	878.3300	2025-07-30
QUW	Mesh, Surgical, Non-Resorbable, Orthopedics, Reinforcement Of Ligament	General, Plastic Surgery	Class 2	878.3300	2025-07-30

Official Correspondent

Christine Scifert

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Theramicro

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K193295	Parcus Medical, LLC	Parcus Knotless PEEK and PEEK CF Push-In Suture Anchor	2020-01-23
K193606	Conmed Corporation	Y-Knot OneStep Anchor	2020-01-22
K984200	R. Thomas Grotz, M.D., Inc.	STABILIZER SOFT TISSUE ANCHOR, 5 AND 8MM; ANCHOR INSERTER, 5 AND 8MM; STABILIZER DRILL, 5 AND 8MM, NONSTERILE; STABILIZE	1999-01-21
K171060	Riverpoint Medical	OrthoButton AL	2017-06-02
K231867	Paragon 28, Inc.	Grappler Suture Anchor System	2023-08-21

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011	Depuy Orthopaedics, Inc.	1	Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

Similar Registrations

Registration Number	Establishment Name	Location
3007923096	Changzhou Biomet Medical Devices Co., Ltd.	Changzhou City Jiangsu, CN
3009417901	SYNTHES GMBH	Zuchwil Solothurn, CH
3006783837	STRUCTURE MEDICAL, LLC.	Naples, FL, US
3003604053	SMITH & NEPHEW INC.	ANDOVER, MA, US
3008870565	Implant Logistics / AMS Micromedical	Sparta, WI, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032412536. Last updated year: 2026. Please use registration number 3032412536 when referencing this establishment in official correspondence.