Data / Medical devices / United States / Seigla Medical, Inc.
Seigla Medical, Inc.: FDA-registered device maker in Buffalo, MN, United States, 2 510(k) clearances
Seigla Medical, Inc. is registered with the FDA (registration 3017708755) in Buffalo, MN, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated April 4, 2025. 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
- 3017708755
- Address
- 7688 5th Street SE, Buffalo, MN, United States, 55313
- Owner or operator
- Seigla Medical, Inc. (10083573)
- Roles
- Specification developer
- First device listed
- November 2, 2022
- Registered through
- 2026
- Brand names listed
- LiquID 051 6F LP, LiquID 051 6F LP Guide Catheter Extension, LiquID 6F Guide Catheter Extension, LiquID 7F Guide Catheter Extension
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Percutaneous | DQY | 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 |
|---|---|---|---|---|---|---|
| April 4, 2025 | K243691 | LiquID .051 LP Guide Catheter Extension | DQY | Substantially Equivalent | Seigla Medical, Inc. | accessdata.fda.gov |
| May 5, 2022 | K220691 | LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension | DQY | Substantially Equivalent | Seigla Medical, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 4, 2025. 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.