Data / Medical devices / Electrosurgical, Cutting & Coagulation & Accessories / Costa Rica
FDA-registered makers of Electrosurgical, Cutting & Coagulation & Accessories in Costa Rica: 8 establishments
8 establishments in Costa Rica are registered with the FDA to make Electrosurgical, Cutting & Coagulation & Accessories (product code GEI). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Electrosurgical, Cutting & Coagulation & Accessories
- Product code
- GEI
- Country
- Costa Rica
Makers of Electrosurgical, Cutting & Coagulation & Accessories in Costa Rica
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Arthrocare Corporation | Coyol Alajuela, Costa Rica | Manufacturer, Repackager or relabeler | 30 | March 30, 2026 | 0 | 0 | 0 | api.fda.gov |
| Deroyal Cientifica De Latinoamerica S.R.L. | La Aurora, Heredia, Costa Rica | Contract manufacturer, Repackager or relabeler | 8 | August 12, 2008 | 0 | 0 | 0 | api.fda.gov |
| Hologic Surgical Products Costa Rica, S.R.L. | El Coyol Alajuela, Costa Rica | Manufacturer | 3 | November 15, 2023 | 0 | 0 | 0 | api.fda.gov |
| ATL Technology CR Limitada | Alajuela, Costa Rica | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomerics Alajuela | Alajuela, Costa Rica | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Freudenberg Medical, SRL | La Garita Alajuela, Costa Rica | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tegra Medical Costa Rica S.A. | La Aurora Heredia, Costa Rica | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Viant Costa Rica, S.A. | Barreal De Heredia, Costa Rica | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.