Data / Medical devices / United States / WestRock Converting, LLC
WestRock Converting, LLC: FDA-registered device maker in Ridgeway, VA, United States, 3 510(k) clearances
WestRock Converting, LLC is registered with the FDA (registration 3005607112) in Ridgeway, VA, United States. It lists 6 device types. The FDA files 3 510(k) clearances under its listings, the newest dated September 15, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005607112
- FEI number
- 3003075526
- Address
- 500 Frith DR., BLDG. A, Ridgeway, VA, United States, 24148
- Owner or operator
- WestRock Converting, LLC (9056422)
- Roles
- Contract manufacturer, Repackager or relabeler
- First device listed
- September 8, 2003
- Registered through
- 2026
- Brand names listed
- Covid-19 face shield, Egens One Step HCG Urine Pregnancy Test Kit(s) (Strip, Cassette, Midstream I and Midstream II), Manual toothbrush, Toothbrush, Toothbrush, Manual, Toothbrush, powered
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Kit, Test, Pregnancy, Hcg, Over The Counter | LCX | 2 | Repackager or relabeler | accessdata.fda.gov |
| Shield, Protective, Personnel | KPY | 1 | Contract manufacturer | accessdata.fda.gov |
| Toothbrush, Ionic, Battery-Powered | MMD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Toothbrush, Powered | JEQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Visual, Pregnancy Hcg, Prescription Use | JHI | 2 | Repackager or relabeler | 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 15, 2014 | K141018 | ORAL-B TEST DRIVE POWER BRUSH TRIAL PROGRAM KIT, ORAL-B TEST DRIVE POWER TOOTHBRUSH KIT, ORAL-B TEST DRIVE REFILL KIT | JEQ | Substantially Equivalent | Procter & Gamble Co. | accessdata.fda.gov |
| February 5, 2013 | K123050 | EGENS ONE STEP HCG URINE PREGNANCY TEST KIT(S) (STRIP, CASSETTE, MIDSTREAM I AND MIDSTREAM II) | LCX | Substantially Equivalent | Nantong Biotechnology Co., Ltd. | accessdata.fda.gov |
| June 5, 2006 | K061351 | ORAL-B SONIC COMPLETE | JEQ | Substantially Equivalent | Braun GmbH | accessdata.fda.gov |
Compare with other makers
- All makers of Toothbrush, Ionic, Battery-Powered
- All makers of Visual, Pregnancy Hcg, Prescription Use
- All makers of Kit, Test, Pregnancy, Hcg, Over The Counter
- All makers of Shield, Protective, Personnel
- All makers of Toothbrush, Powered
- All makers of Toothbrush, Manual
Updated September 15, 2014. 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.