Data / Medical devices / United States / LD Technology LLC
LD Technology LLC: FDA-registered device maker in Miami, FL, United States, 6 510(k) clearances
LD Technology LLC is registered with the FDA (registration 3006146787) in Miami, FL, United States. It lists 5 device types. The FDA files 6 510(k) clearances under its listings, the newest dated May 15, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006146787
- Address
- 990 Biscayne Blvd Ofc O-1403, Miami, FL, United States, 33132
- Owner or operator
- LD TECHNOLOGY LLC (10028854)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- May 4, 2011
- Registered through
- 2026
- Brand names listed
- BP-BT Kiosk, ES-BC, Flow7/CCS Cloud, LD-Oxy, LEDA PAD, Lifeprobes Kiosk, Oxi-w, Smart-abi and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Body Composition | MNW | 2 | Specification developer | accessdata.fda.gov |
| Device, Galvanic Skin Response Measurement | GZO | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | MWI | 2 | Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Plethysmograph, Photoelectric, Pneumatic Or Hydraulic | JOM | 2 | Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Manufacturer, Specification developer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 15, 2020 | K200287 | BP-BT Kiosk | DXN | Substantially Equivalent | Ld Technology, LLC | accessdata.fda.gov |
| April 27, 2020 | K200141 | Oxi-W System | MWI | Substantially Equivalent | Ld Technology, LLC | accessdata.fda.gov |
| December 19, 2017 | K173696 | TBL-ABI System | JOM | Substantially Equivalent | Ld Technology, LLC | accessdata.fda.gov |
| July 6, 2016 | K160956 | LD-Oxi system | MWI | Substantially Equivalent | Ld Technology, LLC | accessdata.fda.gov |
| September 24, 2015 | K152216 | SudoC | GZO | Substantially Equivalent | Ld Technology, LLC | accessdata.fda.gov |
| March 29, 2011 | K103026 | ELECTRO SENSOR -BODY COMPOSITION | MNW | Substantially Equivalent | Ld Technology, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- All makers of Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
- All makers of Analyzer, Body Composition
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Device, Galvanic Skin Response Measurement
Updated May 15, 2020. 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.