Data / Medical devices / Laos / PRIMED Laos Medical Products Manufacturing Sole Co., Ltd.
PRIMED Laos Medical Products Manufacturing Sole Co., Ltd.: FDA-registered device maker in Vientiane Capital Viangchan(Prefecture), Laos, 1 510(k) clearance
PRIMED Laos Medical Products Manufacturing Sole Co., Ltd. is registered with the FDA (registration 3020755815) in Vientiane Capital Viangchan(Prefecture), Laos. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 1, 2026. Registered through 2027. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3020755815
- Address
- Vita Park, Lot No. 73,74,75, KM 22, Ban Nonhthong, Saythany District, Vientiane Capital Viangchan(Prefecture), Laos, 0100
- Owner or operator
- PRIMED Medical Products Inc. (9030179)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- December 12, 2000
- Registered through
- 2027
- Brand names listed
- PRIMAGARD, PRIMASOFT, PRIMED Chemo drug Tested gowns, PRIMED Procedure Masks, PRIMED Surgical Masks, PRIMED Surgical Masks and PRIMED Procedure Masks
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Contract manufacturer | accessdata.fda.gov |
| Gown, Examination | FME | 1 | Contract manufacturer | accessdata.fda.gov |
| Gown, Isolation, Surgical | FYC | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | Contract manufacturer | accessdata.fda.gov |
| Medical Gowns With Chemotherapy Labeling Claims - Tested For Use With Chemotherapy Drugs | QSO | 2 | Manufacturer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Contract manufacturer | accessdata.fda.gov |
| Pediatric/Child Facemask | OXZ | 2 | Contract 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 |
|---|---|---|---|---|---|---|
| September 1, 2026 | K261811 | PRIMED Chemotherapy Drug Tested Gowns (PM4-99450: PRIMED Chemotherapy Drug Tested Isolation Gown, Purple, AAMI Level 2; PM4-99460: PRIMED Chemotherapy Drug Tested Isolation Gown, Blue, AAMI Level 3) | QSO | Substantially Equivalent | PRIMED Medical Products, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Medical Gowns With Chemotherapy Labeling Claims - Tested For Use With Chemotherapy Drugs
- All makers of Gown, Isolation, Surgical
- All makers of Mask, Surgical
- All makers of Pediatric/Child Facemask
- All makers of Non-Surgical Gown
- All makers of Accessory, Surgical Apparel
Updated September 1, 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.