FDA device listing

Collamer UVA PC Introcular Lens

FDA device listing 1596743265 · STAAR SURGICAL Company

Key facts

Proprietary names Collamer UVA PC Introcular Lens
Owner/operator STAAR SURGICAL Company
Owner/operator number 2023826
Premarket submissions P990013
Product codes HQL
Device names HQL - Intraocular Lens
Device class Class III
Classification regulations (21 CFR) 886.3600
Review panels Ophthalmic
Registered establishments STAAR SURGICAL AG, STAAR Surgical Company, STAAR SURGICAL COMPANY
Establishment registrations 2023826, 9614429, 3014173684
FEI numbers 2023826, 3002808259, 3014173684
Establishment operations Manufacturer, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 10–99 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes 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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