FDA applicant

Surgitech C/O Collier, Shannon, Rill & Scott

Washington, DC2 decisions1988–19910 recalls

FDA records 2 decisions for Surgitech C/O Collier, Shannon, Rill & Scott (Washington, DC) from 1988 to 1991: 2 510(k) clearances. Most are in product codes BTO (Tube, Tracheostomy (W/Wo Connector)) and GCJ (Laparoscope, General & Plastic Surgery). 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, anesthesiology panel, where it files most

How often FDA has decided Surgitech C/O Collier, Shannon, Rill & Scott’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Surgitech C/O Collier, Shannon, Rill & Scott since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Surgitech C/O Collier, Shannon, Rill & Scott by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Surgitech”

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

Surgitech, Inc. 2

Surgitech C/O Collier, Shannon, Rill & Scott

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Surgitech”