Data / Medical devices / United States / Invisian Medical LLC
Invisian Medical LLC: FDA-registered device maker in Prairie Village, KS, United States, 1 510(k) clearance
Invisian Medical LLC is registered with the FDA (registration 3023158661) in Prairie Village, KS, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 11, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023158661
- Address
- 7301 Mission Road Suite 215, Prairie Village, KS, United States, 66208
- Owner or operator
- Invisian Medical LLC (10085373)
- Roles
- Manufacturer
- First device listed
- June 9, 2022
- Registered through
- 2026
- Brand names listed
- Minne Ties Agile MMF
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lock, Wire, And Ligature, Intraoral | DYX | 2 | Manufacturer | 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 11, 2017 | K162046 | MINNE TIES MMF Suture System | DYX | Substantially Equivalent | Summit Medical, Inc. | accessdata.fda.gov |
Updated April 11, 2017. 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.