Data / Medical devices / United States / Life PRP
Life PRP: FDA-registered device maker in Dallas, TX, United States, 4 510(k) clearances
Life PRP is registered with the FDA (registration 3033273466) in Dallas, TX, United States. It lists 8 device types. The FDA files 4 510(k) clearances under its listings, the newest dated March 15, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3033273466
- Address
- 2156 W Northwest Hwy Ste 305, Dallas, TX, United States, 75220
- Owner or operator
- Life PRP (10091868)
- Roles
- Complaint file establishment
- First device listed
- November 11, 2024
- Registered through
- 2026
- Brand names listed
- Blood Collection Tube, Vacuum Tube, Diode Laser Therapy System, Electromagnetic Stimulator Device (Model: EM Contouring, Tesla Duet), Genesis AQUALUX, Genesis SOLARA, GeniSculpt, Life PRP Therapeutic Massager, Medical Centrifuge and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Complaint file establishment | accessdata.fda.gov |
| Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use | JQC | 1 | Complaint file establishment | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Complaint file establishment | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Complaint file establishment | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Complaint file establishment | accessdata.fda.gov |
| Powered Microneedle Device | QAI | 2 | Complaint file establishment | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Complaint file establishment | accessdata.fda.gov |
| System, Blood Collection, Vacuum-Assisted, Manual | KST | 1 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| March 15, 2024 | K233307 | Intensity Pulsed Light Therapy System | ONF | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| February 20, 2024 | K231896 | Diode Laser Therapy System | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| August 11, 2023 | K230420 | Dr. pen Microneedling System | QAI | Substantially Equivalent | Guangzhou Ekai Electronic Technology Co., Ltd. | accessdata.fda.gov |
| July 7, 2023 | K231318 | Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet) | NGX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Blood Collection, Vacuum-Assisted, Manual
- All makers of Powered Laser Surgical Instrument
- All makers of Powered Microneedle Device
- All makers of Brush, Dermabrasion, Powered
- All makers of Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
Updated March 15, 2024. 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.