Data / Medical devices / United States / Med Et Al Development Corp.
Med Et Al Development Corp.: FDA-registered device maker in Matthews, NC, United States, 1 510(k) clearance
Med Et Al Development Corp. is registered with the FDA (registration 1058701) in Matthews, NC, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 23, 1995. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1058701
- FEI number
- 1000305409
- Address
- 1226 Mann Dr Ste 200, Matthews, NC, United States, 28105
- Owner or operator
- MED ET AL DEVELOPMENT (9011784)
- Roles
- Manufacturer
- First device listed
- December 10, 2007
- Registered through
- 2027
- Brand names listed
- TGuard
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Finger-Sucking | LQX | 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 |
|---|---|---|---|---|---|---|
| March 23, 1995 | K945537 | T-GUARD | LQX | Substantially Equivalent | Med ET AL Development | accessdata.fda.gov |
Compare with other makers
Updated March 23, 1995. 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.