# Vitaltec Corporation (manufacturer, Taichung, TW): 1 new FDA device listing, incl. tube, tracheostomy (w/wo connector)

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Vitaltec Corporation |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Taichung, TW |
| New listings | 1 |
| Devices | Tube, Tracheostomy (W/Wo Connector) |
| Product codes | BTO |
| Device classes | Class II |
| Medical specialties | Anesthesiology |
| Brand names | Venti-Trach Tracheostomy Tube (570 Series; 571 Series; 580 Series; 581 Series) |
| First new listing | 2026-10-18 |
| Latest new listing | 2026-10-18 |
| FDA registration number | 3040279832 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Listed in the last 45 days.

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.