Data / Medical devices / Bandage, Elastic / Dominican Republic
FDA-registered makers of Bandage, Elastic in the Dominican Republic: 5 establishments
5 establishments in the Dominican Republic are registered with the FDA to make Bandage, Elastic (product code FQM). 0 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
- Bandage, Elastic
- Product code
- FQM
- Country
- Dominican Republic
Makers of Bandage, Elastic in the Dominican Republic
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Deroyal Intercontinental, S.R.L. | Santiago, Dominican Republic | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Garware Healthcare, SAS | Santiago de los Caballeros, Dominican Republic | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Med Paper Dominicana Mepadom SRL | Santo Domingo Oeste, Dominican Republic | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microtek Dominicana, S.A.S. | La Romana, Dominican Republic | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qel Dominicana S.A. | ESPERANZA Valverde, Dominican Republic | Contract manufacturer, 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.