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Innovative Ophthalmic Products, Inc. (Iop)

US Last updated 23 May 2026

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Devices
4
Registries
GUDIDFDA 510(k)
FDA recalls
1

Catalogue4

FDA recalls1

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

  • 2016

    • 22 Feb 2016 Z-1252-2016 Class II Terminated Innovative Ophthalmic Products (IOP) is recalling the Molteno 3 G-Series Glaucoma Implant the package insert/Instructions for Use (IFU) for the device has been updated to add a caution statement to minimize off-label use.

Information

Country
US