Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007142798

FEI Number

3007142798

Entity Name

CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.)

City/State/Country

Woodstock, GA, US

Establishment Address

300 PARKBROOKE PLACE, SUITE 140, Woodstock, GA 30189, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Cordica Medical (Formally Team Technologies, Inc) (Owner Number: 1051594)

Owner / Operator Contact Address

5949 COMMERCE BLVD., --, Morristown, TN 37814, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Topi-CLICK® 35 Dosecheck Troche-CLICK

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HGD	Applicator, Vaginal	Obstetrics/Gynecology	Class 1	884.4520	2019-04-30
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2019-12-27
NXB	Dispenser, Solid Medication	Physical Medicine	Class 1	890.5050	2021-11-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cordica Medical (Formally Team Technologies, Inc)

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3009906207	CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.)	Morgan Hill, CA, US
3007125968	CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.)	Chino, CA, US
3015807001	CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.)	Sunrise, FL, US
3006187135	CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.)	BATAVIA, IL, US
3004713654	CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.)	Haverhill, MA, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K944481	Garan Scientific, Inc.	THE HEART PROTECTOR	1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007142798. Last updated year: 2026. Please use registration number 3007142798 when referencing this establishment in official correspondence.