# Dornier Medtech America, Inc. (other, Kennesaw, GA): 4 new FDA device listings, incl. ureteroscope and accessories, flexible/rigid

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Dornier Medtech America, Inc. |
| Owner / operator | Dornier MedTech America, Inc. |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Kennesaw, GA, US |
| New listings | 4 |
| Devices | Ureteroscope And Accessories, Flexible/Rigid; Powered Laser Surgical Instrument; Laparoscope, General & Plastic Surgery |
| Product codes | FGB, GEX, GCJ |
| Device classes | Class II |
| Medical specialties | Gastroenterology, Urology, General, Plastic Surgery |
| First new listing | 2026-05-22 |
| Latest new listing | 2026-06-12 |
| FDA registration number | 1037955 |
| Registration expires | 2026-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

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.