FDA applicant

Ivory Instruments Co.

Lomita, CA1 decision1988–19880 recalls

FDA records 1 decision for Ivory Instruments Co. (Lomita, CA) in 1988: 1 510(k) clearance. All are in product code HCY (Curette, Uterine). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Ivory Instruments Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ivory Instruments Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Ivory”

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

Ivory Super Holdco Inc. / Zest Anchors, LLC 1 Ivory Super Holdco, Incp. 1 Ivory Gloves Sdn. Bhd. 1

Ivory Instruments Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ivory”