Data / Medical devices / United States / Porex Corporation
Porex Corporation: FDA-registered device maker in Fairburn, GA, United States, 1 510(k) clearance
Porex Corporation is registered with the FDA (registration 1043678) in Fairburn, GA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 2, 1977. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1043678
- Address
- 500 Bohannon Rd, Fairburn, GA, United States, 30213
- Owner or operator
- Porex Corporation (1043678)
- Roles
- Manufacturer
- First device listed
- September 15, 2009
- Registered through
- 2026
- Brand names listed
- FILTER SAMPLER Blood Serum Filter Standard Model, FILTER SAMPLER, BLOOD SERUM FILTER, Fisherband Serum Filters Dispense+ Serum Filter, Fisherband Serum Filters IB Model, Fisherbrand Serum Filters Dispense Filter System, Fisherbrand Serum Filters Instrument Specific Model, Fisherbrand Serum Filters Standard Model, POREX INLINE Reagent Filter and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use | LXG | 1 | Manufacturer | accessdata.fda.gov |
| Tubes, Vacuum Sample, With Anticoagulant | GIM | 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 |
|---|---|---|---|---|---|---|
| November 2, 1977 | K771985 | FILTER SAMPLER BLOOD SERUM FILTER | GIM | Substantially Equivalent | Clasrock | accessdata.fda.gov |
Compare with other makers
- All makers of Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
- All makers of Tubes, Vacuum Sample, With Anticoagulant
Updated November 2, 1977. 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.