Skip to the page
Get started – free

Data / Medical devices / United States / Global TV Concepts, Ltd.

Global TV Concepts, Ltd.: FDA-registered device maker in Coconut Creek, FL, United States, 1 510(k) clearance

Global TV Concepts, Ltd. is registered with the FDA (registration 1063974) in Coconut Creek, FL, United States. It lists 18 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 12, 2014. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this oneWatch Global TV Concepts, Ltd.
FDA registration number
1063974
FEI number
3001739169
Address
6441 Lyons Rd, Coconut Creek, FL, United States, 33073
Owner or operator
GLOBAL TV CONCEPTS, LTD. (9074284)
Roles
Specification developer
First device listed
August 9, 2005
Registered through
2026
Brand names listed
Ankle Brace, Bio Feedbac, Circulation Plus, Circulation Plus Knee, Detox Foot patch, EZ up Cane, Ionic Brush, Knee Brace and more

Devices it lists

DeviceProduct codeClassRoleSource
Adhesive Backed Thermal Skin PatchesOMW1Specification developeraccessdata.fda.gov
Band Or Belt, Pelvic SupportISR1Specification developeraccessdata.fda.gov
Bandage, ElasticFQM1Specification developeraccessdata.fda.gov
Bottle, Hot/Cold WaterFPF1Specification developeraccessdata.fda.gov
Brush, Dermabrasion, PoweredGFE1Specification developeraccessdata.fda.gov
Cane, Safety WalkKHY1Specification developeraccessdata.fda.gov
Epilator, High Frequency, Tweezer-TypeKCX1Specification developeraccessdata.fda.gov
Hearing Aid, Air-Conduction, PrescriptionESD1Specification developeraccessdata.fda.gov
Joint, Ankle, External BraceITW1Specification developeraccessdata.fda.gov
Joint, Knee, External BraceITQ1Specification developeraccessdata.fda.gov
Massager, Therapeutic, ElectricISA1Specification developeraccessdata.fda.gov
Massager, Therapeutic, ManualLYG1Specification developeraccessdata.fda.gov
Orthosis, Limb BraceIQI1Specification developeraccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Specification developeraccessdata.fda.gov
Stimulator, Muscle, Powered, For Muscle ConditioningNGX2Specification developeraccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-CounterNUH2Specification developeraccessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)FQL1Specification developeraccessdata.fda.gov
Unit, Oral IrrigationEFS1Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
November 12, 2014K133929HEALTH EXPERT ELCTRONIC STIMULATORNUHSubstantially EquivalentShenzhen Osto Technology Company Limitedaccessdata.fda.gov

Compare with other makers

Updated November 12, 2014. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.