510(k) Report

FDA applicant

Vector Medical, Inc.

Milton, FL2 decisions2000–20020 recalls

FDA records 2 decisions for Vector Medical, Inc. (Milton, FL) from 2000 to 2002: 2 510(k) clearances. All are in product code HSB (Rod, Fixation, Intramedullary And Accessories). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Vector Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Vector Medical, 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 “Vector”

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