Data / Medical devices / United States / Arlington Specialties, Inc.
Arlington Specialties, Inc.: FDA-registered device maker in Elk Grove Village, IL, United States, 1 510(k) clearance
Arlington Specialties, Inc. is registered with the FDA (registration 3011050481) in Elk Grove Village, IL, United States. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 1, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011050481
- Address
- 1515 Carmen Drive, Elk Grove Village, IL, United States, 60007
- Owner or operator
- Arlington Specialties, Inc. (10047238)
- Roles
- Complaint file establishment, Repackager or relabeler
- First device listed
- May 27, 2016
- Registered through
- 2026
- Brand names listed
- Adhesive Bandage, Headache Cap, Pinch Provisions, SUNGLASSES, Tampax, thermometer
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bag, Ice | KYR | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Floss, Dental | JES | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Strip, Temperature, Forehead, Liquid Crystal | KPD | 2 | Complaint file establishment | accessdata.fda.gov |
| Sunglasses (Non-Prescription Including Photosensitive) | HQY | 1 | Complaint file establishment | accessdata.fda.gov |
| Tampon, Menstrual, Unscented | HEB | 2 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| August 1, 2006 | K061486 | TAMPAX TAMPONS - (LIGHT,REGULAR,SUPER AND SUPER PLUS ABSORBENCIES) | HEB | Substantially Equivalent | Procter & Gamble Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Tape And Bandage, Adhesive
- All makers of Bag, Ice
- All makers of Tampon, Menstrual, Unscented
- All makers of Sunglasses (Non-Prescription Including Photosensitive)
- All makers of Floss, Dental
- All makers of Strip, Temperature, Forehead, Liquid Crystal
Updated August 1, 2006. 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.