FDA applicant

Intermedics Intraocular, Inc.

Freeport, TX4 decisions1983–19860 recalls

FDA records 4 decisions for Intermedics Intraocular, Inc. (Freeport, TX) from 1983 to 1986: 4 510(k) clearances. Most are in product codes KYB (Lens, Guide, Intraocular) and HNW (Dilator, Lachrymal). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Intermedics Intraocular, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intermedics Intraocular, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Intermedics Intraocular, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Intermedics”

FDA records each applicant name separately; these may or may not be the same firm.

Intermedics, Inc. 211 Intermedics Orthopedics 108 Intermedics/Infusaid, Inc. 3

Intermedics Intraocular, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Intermedics”