# Safetec Of America, Inc. (manufacturer, Buffalo, NY): 6 new FDA device listings, incl. accessories, cleaning brushes, for endoscope

**Score:** 95/100

| Field | Value |
|---|---|
| Establishment | Safetec Of America, Inc. |
| Owner / operator | Safetec of America Inc |
| Role | Manufacturer |
| Establishment types | Repack or Relabel Medical Device; Manufacture Medical Device |
| Location | Buffalo, NY, US |
| New listings | 6 |
| Devices | Accessories, Cleaning Brushes, For Endoscope; Cement, Stomal Appliance, Ostomy; Urinary Drainage Collection Kit, For Indwelling Catheter; Scissors, Medical, Disposable; Catheter, Rectal For Continent Ileostomy; Brush, Cleaning, Tracheal Tube |
| Product codes | MNL, EZR, FCN, JOK, KPH, EPE |
| Device classes | Class I, Class II |
| Medical specialties | Gastroenterology, Urology, General Hospital, Anesthesiology |
| Brand names | United Contour Brush Endotracheal 9/16 in. x 16 in. package of 12; United Contour Brushes 1/4 in. x 16 in., package of 12; United Contour Brush Tracheal 9/16 in x 6 in., package of 1 set; United Contour Brush general cleaning set of 8; United Contour Brush set of 3, package of 1 set; United Contour Brush; United Contour Brush Tracheal 3/8 in. x 6 in. Package of 12; United Contour Brush Endotracheal set of 4, package of 1 set |
| First new listing | 2026-06-22 |
| Latest new listing | 2026-09-29 |
| FDA registration number | 1319744 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
- 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: 2026-11-04T21:52:36.524Z.
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.