FDA applicant

Interpore Intl.

Irvine, CA26 decisions1984–19980 recalls

FDA records 26 decisions for Interpore Intl. (Irvine, CA) from 1984 to 1998: 25 510(k) clearances and 1 original PMA approval. Most are in product codes DZE (Implant, Endosseous, Root-Form) and LYC (Bone Grafting Material, Synthetic). Its devices cite 5 predicates, 1 of them its own earlier devices. 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, dental panel, where it files most

How often FDA has decided Interpore Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Interpore Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Interpore”

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

Interpore Cross Intl. 39

Interpore Intl.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Interpore”