FDA applicant

Abbott Vascular (Idef Technologies Inc)

Santa Clara1 decision2014–20140 recalls

FDA records 1 decision for Abbott Vascular (Idef Technologies Inc) (Santa Clara) in 2014: 1 original PMA approval. All are in product code NIP (Stent, Superficial Femoral Artery). 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, cardiovascular panel, where it files most

How often FDA has decided Abbott Vascular (Idef Technologies Inc)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Abbott Vascular (Idef Technologies Inc) by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Abbott”

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

Abbott Laboratories 920 Abbott Medical 92 Abbott Vascular 64 Abbott Diabetes Care, Inc. 42 Abbott Molecular, Inc. 33 Abbott Diagnostics 28 Abbott Point of Care, Inc. 22 Abbott Medical Optics, Inc. 16 Abbott Mfg., Inc. 14 Abbott 14 Abbott Spine, Inc. 13 Abbott Diagnostics Scarborough, Inc. 8

Abbott Vascular (Idef Technologies Inc)

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Abbott”