Data / Medical devices / United States / Sun Pharmaceutical Industries, Inc.
Sun Pharmaceutical Industries, Inc.: FDA-registered device maker in Billerica, MA, United States, 1 PMA approval
Sun Pharmaceutical Industries, Inc. is registered with the FDA (registration 1226354) in Billerica, MA, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated December 3, 1999. 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
- 1226354
- FEI number
- 3002513708
- Address
- 29 Dunham Road, Billerica, MA, United States, 01821
- Owner or operator
- DUSA PHARMACEUTICALS, INC. (9039997)
- Roles
- Manufacturer, Specification developer
- First device listed
- January 1, 2008
- Registered through
- 2026
- Brand names listed
- BLU-U, BLU-U Model 4170
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Laser, Photodynamic Therapy | MVF | 3 | Manufacturer, Specification developer | 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 |
|---|---|---|---|---|---|---|
| December 3, 1999 | P990019 | BLU -U BLUE LIGHT PHOTODYNAMIC THERAPY ILLUMINATOR | MVF | 8 | May 1, 2025 | accessdata.fda.gov |
Compare with other makers
Updated May 1, 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.