FDA applicant

Twin Falls Orthopedic Associates, P.A.

Twin Falls, ID1 decision1986–19860 recalls

FDA records 1 decision for Twin Falls Orthopedic Associates, P.A. (Twin Falls, ID) in 1986: 1 510(k) clearance. All are in product code HRX (Arthroscope). 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 Twin Falls Orthopedic Associates, P.A.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Twin Falls Orthopedic Associates, P.A. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Twin Falls Orthopedic Associates, P.A. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Twin Falls Orthopedic Associates, P.A.’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 “Twin”

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

Twin City Surgical, Inc. 6 Twin Star Medical, Inc. 4

Twin Falls Orthopedic Associates, P.A.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Twin”