Data / Medical devices / United States / Menasha Packaging Company, LLC
Menasha Packaging Company, LLC: FDA-registered device maker in Lebanon, PA, United States, 1 510(k) clearance
Menasha Packaging Company, LLC is registered with the FDA (registration 3021035729) in Lebanon, PA, United States. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 29, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021035729
- Address
- 3100 State Drive Suite 200, Lebanon, PA, United States, 17042
- Owner or operator
- Menasha Packaging Co. LLC (10045291)
- Roles
- Repackager or relabeler
- First device listed
- November 4, 2013
- Registered through
- 2026
- Brand names listed
- First Aid Kit, First aid kit with drug, Floss, Dental, Varnish, Cavity, tape and bandage, adhesive
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Occlusive | NAD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Fiber, Medical, Absorbent | FRL | 1 | Repackager or relabeler | accessdata.fda.gov |
| First Aid Kit With Drug | LRR | N | Repackager or relabeler | accessdata.fda.gov |
| Floss, Dental | JES | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Varnish, Cavity | LBH | 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 |
|---|---|---|---|---|---|---|
| January 29, 2015 | K143155 | LISTERINE Sensitivity Defense Mouthrinse | LBH | Substantially Equivalent | Johnson & Johnson Healthcare Products, Division of Mcneil-Pp | accessdata.fda.gov |
Compare with other makers
- All makers of Floss, Dental
- All makers of Dressing, Wound, Occlusive
- All makers of Fiber, Medical, Absorbent
- All makers of Varnish, Cavity
- All makers of Tape And Bandage, Adhesive
- All makers of First Aid Kit With Drug
Updated January 29, 2015. 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.