FDA applicant

Bend Orthopedic & Fracture Clinic

Mchenry, IL1 decision1980–19800 recalls

FDA records 1 decision for Bend Orthopedic & Fracture Clinic (Mchenry, IL) in 1980: 1 510(k) clearance. All are in product code FWZ (Operating Room Accessories Table Tray). 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, general and plastic surgery panel, where it files most

How often FDA has decided Bend Orthopedic & Fracture Clinic’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bend Orthopedic & Fracture Clinic since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bend Orthopedic & Fracture Clinic by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Bend”

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

Bend IT Technologies, Ltd. 4

Bend Orthopedic & Fracture Clinic

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bend”