Data / Medical devices / Electrophoretic, Protein Fractionation
Electrophoretic, Protein Fractionation (CEF): 7 FDA-registered makers in 5 countries
7 establishments in 5 countries are registered with the FDA to make Electrophoretic, Protein Fractionation (product code CEF, Class 1, 21 CFR 862.1630). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 29 510(k) clearances under this code, the latest on July 26, 2013, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- CEF
- Device class
- 1
- Regulation
- 862.1630
- Medical specialty
- Clinical Chemistry
Makers by country
| Country | Makers |
|---|---|
| United States | 2 |
| United Kingdom | 2 |
| France | 1 |
| Italy | 1 |
| Netherlands | 1 |
Makers of Electrophoretic, Protein Fractionation
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Helena Laboratories, Corp. | Beaumont, TX, United States | Manufacturer | 1 | October 27, 1997 | 0 | 0 | 0 | api.fda.gov |
| Helena Laboratories, Corp. | Beaumont, TX, United States | Manufacturer | 1 | October 27, 1997 | 0 | 0 | 0 | api.fda.gov |
| Sebia | EVRY Essonne, France | Manufacturer | 1 | July 26, 2013 | 0 | 0 | 0 | api.fda.gov |
| Helena Laboratories UK Ltd | Gateshead Newcastle upon Tyne, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Interlab S.R.L. | ROME Lazio, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Prince Technologies B.V. | Emmen Drenthe, Netherlands | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Binding Site Group Ltd. | Birmingham, United Kingdom | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated July 26, 2013. 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.