Contract manufacturerSEKO MedTec Solutions (Oakdale, PA)PennsylvaniaOrthopedicClass II
SEKO MedTec Solutions
Contract manufacturer · Oakdale, PA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3010032952 (openFDA record; or search FDA's registration database)
- FEI number
- 3010032952
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer; Repackager or relabeler
- Owner or operator
- SEKO MedTec Solutions (FDA owner/operator no. 10042726)
- Registered address
- 300 Crown Court, Suite 320, Oakdale, PA 15071
- Contract listings
- 1 device listings, 1 product codes, first listed Jan 22, 2021
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| LOF | Stimulator, Bone Growth, Non-Invasive | Class II | Orthopedic | Contract manufacturing | Jan 22, 2021 |