# Beyonics International PTE. Ltd. (contract manufacturer, SINGAPORE North West, SG): 5 new FDA device listings, incl. sacroiliac joint guidewire placement device

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Beyonics International PTE. Ltd. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | SINGAPORE North West, SG |
| New listings | 5 |
| Devices | Sacroiliac Joint Guidewire Placement Device; Stimulator, Nerve; Neurosurgical Nerve Locator |
| Product codes | SCY, ETN, PDQ |
| Device classes | Class II |
| Medical specialties | Orthopedic, Ear, Nose, Throat |
| Brand names | Cannulated PsiFGuard; PediGuard Threaded; DSG Connect Technology |
| First new listing | 2026-08-31 |
| Latest new listing | 2026-08-31 |
| FDA registration number | 3003080184 |
| 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: 2026-11-04T21:52:36.524Z.
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.