Data / Medical devices / Dominican Republic / Remington Medical, S.A.
Remington Medical, S.A.: FDA-registered device maker in Santo Domingo Este, Dominican Republic, 5 510(k) clearances
Remington Medical, S.A. is registered with the FDA (registration 3009265194) in Santo Domingo Este, Dominican Republic. It lists 13 device types. The FDA files 5 510(k) clearances under its listings, the newest dated November 20, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009265194
- Address
- Zona Franca Industrial de las Americas, Edificio B-11 Km. 22 Autopista Las Americas, Santo Domingo Este, Dominican Republic, 15001
- Owner or operator
- REMINGTON MEDICAL, INC. (9006473)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- February 28, 2006
- Registered through
- 2026
- Brand names listed
- 10cc Locking Syringe, 301-CG Family, ADAP-1 Family, ADAP-2 Family, ADAP-2000 Family, ADAP-2R Family, ADAP-2RL Family, Aspiration and Injection Needles and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 20, 2025 | K251904 | VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01) | DPW | Substantially Equivalent | Remington Medical, Inc. | accessdata.fda.gov |
| July 12, 2019 | K191315 | Remington Medical, Inc. Automatic Cutting Needle (NAC) | KNW | Substantially Equivalent | Remington Medical, Inc. | accessdata.fda.gov |
| November 3, 1998 | K983621 | NEEDLE GUIDE | IZH | Substantially Equivalent | Remington Medical, Inc. | accessdata.fda.gov |
| September 8, 1998 | K982401 | PROSTATE BIOPSY NEEDLE | KNW | Substantially Equivalent | Remington Medical, Inc. | accessdata.fda.gov |
| September 29, 1994 | K943651 | TECHNA-CUT ASPIRATION NEEDLE | KNW | Substantially Equivalent | Manan Medical Products, Inc. | accessdata.fda.gov |
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Updated November 20, 2025. 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.