Data / Medical devices / United States / American Health Packaging
American Health Packaging: FDA-registered device maker in Columbus, OH, United States, 1 510(k) clearance
American Health Packaging is registered with the FDA (registration 3000209995) in Columbus, OH, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 6, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3000209995
- Address
- 2550 John Glenn Ave Ste A, Columbus, OH, United States, 43217
- Owner or operator
- American Health Packaging (10052971)
- Roles
- Complaint file establishment, Repackager or relabeler, Reprocessor
- First device listed
- December 22, 2025
- Registered through
- 2026
- Brand names listed
- AHP Prefilled Syringe
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dispenser, Liquid Medication | KYX | 1 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Enteral Syringes With Enteral Specific Connectors | PNR | 2 | Complaint file establishment, Reprocessor | 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 6, 2019 | K190502 | ENFit Oral / Enteral Syringe | PNR | Substantially Equivalent | Jiangsu Caina Medical Co.,Ltd | accessdata.fda.gov |
Compare with other makers
- All makers of Dispenser, Liquid Medication
- All makers of Enteral Syringes With Enteral Specific Connectors
Updated August 6, 2019. 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.