Data / Medical devices / Arthroscope / Costa Rica
FDA-registered makers of Arthroscope in Costa Rica: 5 establishments
5 establishments in Costa Rica are registered with the FDA to make Arthroscope (product code HRX). 2 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
- Arthroscope
- Product code
- HRX
- Country
- Costa Rica
Makers of Arthroscope 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 | 9 | June 28, 2001 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Medical Costa Rica S.R.L. | Coyol Alajuela, Costa Rica | Manufacturer | 1 | November 10, 1999 | 0 | 0 | 0 | api.fda.gov |
| Baxter Productos Medicos, Ltda. | 1-7052 Cartago, Costa Rica | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomerics Alajuela | Alajuela, Costa Rica | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nitinol Devices & Components Costa Rica, S. R. L. | El Coyol Alajuela, 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.