FDA applicant

Enteric Medical Technologies

Foster City, CA3 decisions2000–20020 recalls

FDA records 3 decisions for Enteric Medical Technologies (Foster City, CA) from 2000 to 2002: 3 510(k) clearances. All are in product code FBK (Endoscopic Injection Needle…). No recall is linked to its devices.

FDA’s records also spell it “Enteric Medical Technologies, Inc.”.

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

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Enteric Medical Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Enteric Medical Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Enteric”

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

Enteric Products, Inc. 2

Enteric Medical Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Enteric”