Data / Medical devices / United States / Venoscope, LLC
Venoscope, LLC: FDA-registered device maker in Lafayette, LA, United States, 1 510(k) clearance
Venoscope, LLC is registered with the FDA (registration 2319429) in Lafayette, LA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 16, 1994. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2319429
- FEI number
- 1000306918
- Address
- 1018 Harding ST Ste 104, Lafayette, LA, United States, 70503
- Owner or operator
- VENOSCOPE, LLC (9010689)
- Roles
- Manufacturer
- First device listed
- March 5, 2020
- Registered through
- 2026
- Brand names listed
- Venoscope NT01, Venoscope VT03
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Transilluminator, Battery-Powered | HJN | 1 | 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 |
|---|---|---|---|---|---|---|
| May 16, 1994 | K941035 | VENOSCOPE | HJN | Substantially Equivalent | Trinity Partners, LLC | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| April 28, 2005 | 36548 | Not yet classified | Terminated | Venoscope Neonatal Transilluminator, Model NT01 | Excessive heating due to incorrect wire assembly process. | accessdata.fda.gov |
Compare with other makers
Updated October 28, 2006. 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.