Data / Medical devices / United States / Pharma Packaging Solutions, LLC dba Tjoapack, LLC
Pharma Packaging Solutions, LLC dba Tjoapack, LLC: FDA-registered device maker in Clinton, TN, United States, 1 PMA approval
Pharma Packaging Solutions, LLC dba Tjoapack, LLC is registered with the FDA (registration 3002763532) in Clinton, TN, United States. It lists 2 device types. The FDA files 1 PMA approval under its listings, the newest dated January 17, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002763532
- Address
- 341 JD Yarnell Industrical Parkway, Clinton, TN, United States, 37716
- Owner or operator
- Pharma Packaging Solutions, LLC dba Tjoapack, LLC (10059412)
- Roles
- Contract manufacturer, Repackager or relabeler
- First device listed
- June 14, 2021
- Registered through
- 2026
- Brand names listed
- Lumitrace Injection - 10 vials, Lumitrace Injection - 50 vials
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Syringe, Piston | FMF | 2 | Contract manufacturer | accessdata.fda.gov |
| Transdermal Test For Assessment Of Glomerular Filtration Rate | SDK | 3 | Repackager or relabeler | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| January 17, 2025 | P230019 | MediBeacon® Transdermal GFR Measurement System (TGFR) | SDK | 4 | October 2, 2026 | accessdata.fda.gov |
Compare with other makers
- All makers of Transdermal Test For Assessment Of Glomerular Filtration Rate
- All makers of Syringe, Piston
Updated October 2, 2026. 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.