Data / Medical devices / United States / Lohman Technologies, LLC
Lohman Technologies, LLC: FDA-registered device maker in Pewaukee, WI, United States, 1 510(k) clearance
Lohman Technologies, LLC is registered with the FDA (registration 3012267350) in Pewaukee, WI, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 23, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012267350
- Address
- N27W23953 Paul Rd Ste 204, Pewaukee, WI, United States, 53072
- Owner or operator
- Lohman Technologies, LLC (10050825)
- Roles
- Manufacturer
- First device listed
- December 31, 2015
- Registered through
- 2026
- Brand names listed
- homECG+
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Transmitters And Receivers, Electrocardiograph, Telephone | DXH | 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 |
|---|---|---|---|---|---|---|
| June 23, 2006 | K052767 | AFIBALERT ATRIAL FIBRILLATION DETECTOR | DXH | Substantially Equivalent | Lechnologies Research, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 23, 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.