Data / Medical devices / United States / Dealmed
Dealmed: FDA-registered device maker in Lakewood, NJ, United States, 2 510(k) clearances
Dealmed is registered with the FDA (registration 3009761558) in Lakewood, NJ, United States. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 10, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009761558
- Address
- 600 James Street, Lakewood, NJ, United States, 08701
- Owner or operator
- DEALMED MEDICAL SUPPLIES LLC (10041711)
- Roles
- Repackager or relabeler
- First device listed
- December 28, 2021
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bandage, Elastic | FQM | 1 | Repackager or relabeler | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Repackager or relabeler | accessdata.fda.gov |
| Pad, Alcohol, Device Disinfectant | LKB | U | Repackager or relabeler | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Repackager or relabeler | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| February 10, 2006 | K060211 | WUZHOU SYRINGE, WITH/WITHOUT NEEDLE | FMF | Substantially Equivalent | Wenzhou Wuzhou Group Co. , Ltd. | accessdata.fda.gov |
| October 7, 1995 | K951254 | SAFETYGLIDE NEEDLE | FMI | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Piston
- All makers of Pad, Alcohol, Device Disinfectant
- All makers of Bandage, Elastic
- All makers of Needle, Hypodermic, Single Lumen
Updated February 10, 2006. 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.