# Molex (Thailand) Ltd. (contract manufacturer, Bangpakong Chachoengsao, TH): 5 new FDA device listings, incl. stimulator, spinal-cord, totally implanted for pain relief

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Molex (Thailand) Ltd. |
| Owner / operator | Molex (Thailand) Limited |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Bangpakong Chachoengsao, TH |
| New listings | 5 |
| Devices | Stimulator, Spinal-Cord, Totally Implanted For Pain Relief; Catheter, Electrode Recording, Or Probe, Electrode Recording; Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation; Cable, Transducer And Electrode, Patient, (Including Connector) |
| Product codes | LGW, DRF, QZI, DSA |
| Device classes | Class II, Class III |
| Medical specialties | Cardiovascular |
| Brand names | SCS EPG Header and Sterile Cable Kit; Current™ PFA Unified Cable |
| First new listing | 2026-06-29 |
| Latest new listing | 2026-08-14 |
| FDA registration number | 3012693387 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.