Data / Medical devices / Denmark / Powermedic Aps
Powermedic Aps: FDA-registered device maker in HOLBAEK Sjaelland, Denmark, 2 510(k) clearances
Powermedic Aps is registered with the FDA (registration 3003889343) in HOLBAEK Sjaelland, Denmark. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated May 2, 2014. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3003889343
- Address
- 8 Gasvaerksvej, HOLBAEK Sjaelland, Denmark, 4300
- Owner or operator
- PowerMedic Worldwide SL (10094726)
- Roles
- Manufacturer
- First device listed
- December 18, 2025
- Registered through
- 2026
- Brand names listed
- GigaLaser, PowerLaser
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 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 |
|---|---|---|---|---|---|---|
| May 2, 2014 | K134017 | GIGALASER | ILY | Substantially Equivalent | Powermedic Aps | accessdata.fda.gov |
| July 2, 2007 | K070516 | POWERLASER | ILY | Substantially Equivalent | Powermedic Aps | accessdata.fda.gov |
Compare with other makers
Updated May 2, 2014. 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.