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Data / Medical devices / Phakic Toric Intraocular Lens

Phakic Toric Intraocular Lens (QCB): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Phakic Toric Intraocular Lens (product code QCB, Class 3, 21 CFR 886.3600). 0 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
QCB
Device class
3
Regulation
886.3600
Medical specialty
Ophthalmic
Implant
Yes

Makers by country

CountryMakers
United States2
Switzerland1

Makers of Phakic Toric Intraocular Lens

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Staar Surgical AGNIDAU Bern, SwitzerlandManufacturer0010api.fda.gov
Staar Surgical CompanyMonrovia, CA, United StatesManufacturer, Specification developer0010api.fda.gov
STAAR Surgical CompanyTustin, CA, United StatesSpecification developer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.