Contract manufacturerSanbor Medical (Allentown, PA)PennsylvaniaAnesthesiologyNeurologyClass II
Sanbor Medical
Contract manufacturer ยท Allentown, PA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3007113169 (openFDA record; or search FDA's registration database)
- FEI number
- 3007113169
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Contract manufacturer
- Owner or operator
- Sanbor Medical (FDA owner/operator no. 10028522)
- Registered address
- 7584 Morris Court, Suite 218, Allentown, PA 18106
- Contract listings
- 2 device listings, 2 product codes, first listed Feb 22, 2016
- 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 |
|---|---|---|---|---|---|
| BZG | Spirometer, Diagnostic | Class II | Anesthesiology | Contract manufacturing | Feb 22, 2016 |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | Class II | Neurology | Contract manufacturing | Sep 13, 2023 |