Data / Medical devices / Netherlands / Nordic Pharma BVG
Nordic Pharma BVG: FDA-registered device maker in Siriusdreef, Netherlands, 1 PMA approval
Nordic Pharma BVG is registered with the FDA (registration 3039186269) in Siriusdreef, Netherlands. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated July 16, 1998. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3039186269
- Address
- Siriusdreef 41 2132 WT Hoofddorp, Siriusdreef, Netherlands, 41
- Owner or operator
- Nordic Pharma BV (10095781)
- Roles
- Specification developer
- First device listed
- April 28, 2026
- Registered through
- 2026
- Brand names listed
- Biolon
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Aid, Surgical, Viscoelastic | LZP | 3 | 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 |
|---|---|---|---|---|---|---|
| July 16, 1998 | P960011 | BIOLON 1% SODIUM HYALURONATE VISCOELASTIC SURGICAL AID FLUID | LZP | 33 | October 3, 2022 | accessdata.fda.gov |
Compare with other makers
Updated October 3, 2022. 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.