Data / Medical devices / United States / Pegasus Imports
Pegasus Imports: FDA-registered device maker in Houston, TX, United States, 2 510(k) clearances
Pegasus Imports is registered with the FDA (registration 3029328631) in Houston, TX, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 25, 2016. 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.
- FDA registration number
- 3029328631
- Address
- 4000 Airline Dr., STE D, Houston, TX, United States, 77022
- Owner or operator
- Pegasus Imports (10088744)
- Roles
- Specification developer
- First device listed
- October 6, 2023
- Registered through
- 2026
- Brand names listed
- Livaclean Health Insulin Syringe, Livaclean Health Pen Needles
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Hypodermic, Single Lumen | FMI | 2 | Specification developer | accessdata.fda.gov |
| Syringe, Antistick | MEG | 2 | Specification developer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | 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 |
|---|---|---|---|---|---|---|
| March 25, 2016 | K152808 | U&U Insulin Syringe with/without Safety Retractable Device | MEG | Substantially Equivalent | U&U Medical Technology Co, Ltd. | accessdata.fda.gov |
| May 29, 2014 | K131954 | MEDI PEN NEEDLE | FMI | Substantially Equivalent | Shanghai Carelife International Trading Co. , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Piston
- All makers of Syringe, Antistick
- All makers of Needle, Hypodermic, Single Lumen
Updated March 25, 2016. 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.