FDA device listing

Diff Eyewear,Dime Optics,Lime Optical Company

FDA device listing 1314090692 · DIFF, LLC

Key facts

Proprietary names Diff Eyewear,Dime Optics,Lime Optical Company
Owner/operator DIFF, LLC
Owner/operator number 10052532
Product codes HOI
Device names HOI - Spectacle, Magnifying
Device class Class I
Classification regulations (21 CFR) 886.5840
Review panels Ophthalmic
Registered establishments DIFF, LLC
Establishment registrations 3012498117
FEI numbers 3012498117
Establishment operations Specification Developer
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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