Data / Medical devices / Netherlands / GATT Technologies BV
GATT Technologies BV: FDA-registered device maker in Nijmegen Gelderland, Netherlands, 1 PMA approval
GATT Technologies BV is registered with the FDA (registration 3023251262) in Nijmegen Gelderland, Netherlands. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated December 15, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023251262
- Address
- Transistorweg 5, Nijmegen Gelderland, Netherlands, 6534 AT
- Owner or operator
- ETHICON INC. (2210968)
- Roles
- Manufacturer
- First device listed
- December 16, 2025
- Registered through
- 2026
- Brand names listed
- ETHIZIA Hemostatic Patch
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Agent, Absorbable Hemostatic, Collagen With Polymeric Additives | SGV | 3 | 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 |
|---|---|---|---|---|---|---|
| December 15, 2025 | P240035 | ETHIZIA | SGV | 6 | August 27, 2026 | accessdata.fda.gov |
Updated August 27, 2026. 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.