Data / Medical devices / United Kingdom / Molecular Products Ltd
Molecular Products Ltd: FDA-registered device maker in HARLOW Essex, United Kingdom, 1 510(k) clearance
Molecular Products Ltd is registered with the FDA (registration 3002807637) in HARLOW Essex, United Kingdom. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 6, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002807637
- Address
- Parkway Harlow Business Park, HARLOW Essex, United Kingdom, CM19 5FR
- Owner or operator
- MOLECULAR PRODUCTS LTD. (9005230)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- April 17, 1992
- Registered through
- 2026
- Brand names listed
- Rugged Oxygen Generator (ROG), SOFNOLIME, SUPERIA, SoLo, Sodasorb
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Absorbent, Carbon-Dioxide | CBL | 1 | Manufacturer | accessdata.fda.gov |
| Absorber, Carbon-Dioxide | BSF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Generator, Oxygen, Portable | CAW | 2 | 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 |
|---|---|---|---|---|---|---|
| December 6, 2024 | K240561 | Rugged Oxygen Generator (ROG) (RO01-00001) | CAW | Substantially Equivalent | Molecular Products , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Absorber, Carbon-Dioxide
- All makers of Absorbent, Carbon-Dioxide
- All makers of Generator, Oxygen, Portable
Updated December 6, 2024. 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.