Data / Medical devices / United States / Technicuff Corp.
Technicuff Corp.: FDA-registered device maker in Leesburg, FL, United States, 1 510(k) clearance
Technicuff Corp. is registered with the FDA (registration 1058002) in Leesburg, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 6, 1994. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1058002
- FEI number
- 1000222013
- Address
- 2525 Industrial St., Leesburg, FL, United States, 34748
- Owner or operator
- TECHNICUFF CORP. (9010195)
- Roles
- Manufacturer
- First device listed
- January 2, 2008
- Registered through
- 2026
- Brand names listed
- Technicuff Blood Pressure Cuff
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Pressure Cuff | DXQ | 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 |
|---|---|---|---|---|---|---|
| September 6, 1994 | K942259 | TECHNICUFF | DXQ | Substantially Equivalent | Technicuff Corp. | accessdata.fda.gov |
Compare with other makers
Updated September 6, 1994. 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.