FDA applicant

Pillar Surgical, Inc.

La Jolla, CA7 decisions1995–20000 recalls

FDA records 7 decisions for Pillar Surgical, Inc. (La Jolla, CA) from 1995 to 2000: 7 510(k) clearances. Most are in product codes MIC (Implant, Muscle, Pectoralis) and MDA (Elastomer, Silicone, For Scar Management). Its devices cite 4 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Pillar Surgical”.

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

FIG. A — Illustration, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Pillar Surgical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pillar Surgical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Pillar”

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

Pillar Technology, Inc. 6 Pillar Biosciences 1

Pillar Surgical, Inc.

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 “Pillar”