Data / Medical devices / United States / Serb Medical Solutions Inc.
Serb Medical Solutions Inc.: FDA-registered device maker in Hattiesburg, MS, United States, 1 510(k) clearance
Serb Medical Solutions Inc. is registered with the FDA (registration 3009169861) in Hattiesburg, MS, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 25, 2003. 1 recall event names it as the recalling firm (1 Class I). Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009169861
- Address
- 46 Shelby Thames Drive, Hattiesburg, MS, United States, 39402
- Owner or operator
- Serb Medical Solutions Inc (10093886)
- Roles
- Manufacturer
- First device listed
- July 29, 2025
- Registered through
- 2026
- Brand names listed
- RSDL
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Decontamination Kit | MAC | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| March 25, 2003 | K023969 | REACTIVE SKIN DECONTAMINATION LOTION | MAC | Substantially Equivalent | Dept. of the Army | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| November 24, 2022 | 91336 | Class I | Terminated | RSDL (Reactive Skin Decontamination Lotion) Kit, NSN 6505-21-912-5229. Used to remove and/or neutralize chemical warfare agents and T-2 Toxin from the skin. | Complaints of leaking packets were received. | accessdata.fda.gov |
Compare with other makers
Updated January 10, 2023. 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.