FDA device listing

Lamarca,TRIS OTTICA SPA

FDA device listing 1264020724 · Trisottica Srl

Key facts

Proprietary names Lamarca,TRIS OTTICA SPA
Owner/operator Trisottica Srl
Owner/operator number 10078799
Product codes HQY
Device names HQY - Sunglasses (Non-Prescription Including Photosensitive)
Device class Class I
Classification regulations (21 CFR) 886.5850
Review panels Ophthalmic
Registered establishments TRIS OTTICA SPA
Establishment registrations 3003085967
FEI numbers 3003085967
Establishment operations Foreign Exporter, Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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