Data / Medical devices / Trinidad and Tobago
Medical device makers in Trinidad and Tobago: 1 FDA-registered establishment
1 establishment in Trinidad and Tobago are registered with the FDA to make medical devices for the US market, listing 5 device types. 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Country
- Trinidad and Tobago
Device types made here
Device types with the most registered makers in this country.
| Device | Product code | Makers |
|---|---|---|
| Device, Anti-Snoring | LRK | 1 |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 1 |
| Denture, Plastic, Teeth | ELM | 1 |
| Clasp, Preformed | EHP | 1 |
| Additively Manufactured, Preformed, Resin Denture Tooth | PZY | 1 |
Makers in Trinidad and Tobago
Best documented first: most 510(k) clearances and PMA approvals.
| Maker | Location | Device types | 510(k) clearances | PMA approvals | Recall events | Source |
|---|---|---|---|---|---|---|
| The Myerson Company Limited | Laventille San JuanLaventille, Trinidad and Tobago | 5 | 8 | 0 | 0 | api.fda.gov |
Updated November 3, 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.