Data / Medical devices / Finland / Modulight Corporation
Modulight Corporation: FDA-registered device maker in Tampere Pirkanmaa, Finland, 1 PMA approval
Modulight Corporation is registered with the FDA (registration 3006268530) in Tampere Pirkanmaa, Finland. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated April 4, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006268530
- Address
- Hermiankatu 22, Tampere Pirkanmaa, Finland, 33720
- Owner or operator
- Modulight Corporation (10052625)
- Roles
- Contract manufacturer, Contract sterilizer, Manufacturer
- First device listed
- August 30, 2016
- Registered through
- 2026
- Brand names listed
- ML7710, ML7710-630-PIN, Modulight ML6710i Laser, Photofrin 630 PDT laser
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Laser, Photodynamic Therapy | MVF | 3 | Contract manufacturer, Contract sterilizer, Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| April 4, 2006 | P050026 | QUANTEL ACTIVIS LASER AND ZSL30 ACT, ZSL120 ACT, AND HSBMBQ ACT SLIT LAMP ADAPTERS | MVF | 3 | February 11, 2025 | accessdata.fda.gov |
Compare with other makers
Updated February 11, 2025. 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.