# Karl Storz Endoscopy-America, Inc. (other, El Segundo, CA): 15 new FDA device listings, incl. endoscopic grasping/cutting instrument, non-powered

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Karl Storz Endoscopy-America, Inc. |
| Owner / operator | Karl Storz Se & Co Kg |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | El Segundo, CA, US |
| New listings | 15 |
| Devices | Endoscopic Grasping/Cutting Instrument, Non-Powered; Arthroscope; Laparoscope, General & Plastic Surgery; Hysteroscope (And Accessories); Laryngoscope, Nasopharyngoscope; Insufflator, Endoscopic Vessel Harvesting; Insufflator, Laparoscopic; Pump, Portable, Aspiration (Manual Or Powered); Nasopharyngoscope (Flexible Or Rigid); System, Irrigation, Urological |
| Product codes | OCZ, HRX, GCJ, HIH, EQN, OSV, HIF, BTA, EOB, LJH, HIG, OCX |
| Device classes | Class II |
| Medical specialties | Gastroenterology, Urology, Orthopedic, Obstetrics/Gynecology, Ear, Nose, Throat, General, Plastic Surgery |
| Brand names | KARL STORZ Endoscopic Accessories for Urology; HOPKINS Telescopes for Arthroscopy; KARL STORZ Trocars with Valve Seals; UNIDRIVE Select System; KARL STORZ Laryngoscopes and Accessories; Smart Smoke Evacuation; ENDOFLATOR +; ENDOMAT SELECT |
| First new listing | 2026-06-17 |
| Latest new listing | 2026-09-28 |
| FDA registration number | 3010202439 |
| Registration expires | 2027-12-31 |

## Why this score
- 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.