FDA applicant

Intera Corp.

Chattanooga, TN6 decisions1986–19891 recall

FDA records 6 decisions for Intera Corp. (Chattanooga, TN) from 1986 to 1989: 6 510(k) clearances. Most are in product codes EYQ (Garment, Protective, For Incontinence) and KKX (Drape, Surgical, Antimicrobial). 1 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Intera Corp. since 2007.

Recalls per year

1in 2011

2007high 1 (2011) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Intera”

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

Intera Oncology, Inc. 4

Intera Corp.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Intera”