Data / Medical devices / United States / US Paper Mill LLC
US Paper Mill LLC: FDA-registered device maker in Chillicothe, OH, United States, 1 510(k) clearance
US Paper Mill LLC is registered with the FDA (registration 3043739177) in Chillicothe, OH, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 13, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043739177
- Address
- 232 E 8th St, Chillicothe, OH, United States, 45601
- Owner or operator
- US Medical Glove Company (10084518)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- January 31, 2023
- Registered through
- 2026
- Brand names listed
- Nitrile Exam Glove (Chemotherapy Drug Tested)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Medical Glove, Specialty | LZC | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy Drugs | OPJ | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Polymer Patient Examination Glove | LZA | 1 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| January 13, 2023 | K223748 | Nitrile Exam Gloves (Chemotherapy Drug Tested) | LZA | Substantially Equivalent | Us Medical Glove Company, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Medical Glove, Specialty
- All makers of Polymer Patient Examination Glove
- All makers of Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy Drugs
Updated January 13, 2023. 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.