FDA applicant

Ortho Pared Instruments, Inc.

Mchenry, IL4 decisions1981–19830 recalls

FDA records 4 decisions for Ortho Pared Instruments, Inc. (Mchenry, IL) from 1981 to 1983: 4 510(k) clearances. Most are in product codes HRX (Arthroscope) and HTZ (Instrument, Cutting, Orthopedic). 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 Ortho Pared Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ortho Pared Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Ortho”

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

Ortho-Clinical Diagnostics, Inc. 152 Ortho Diagnostic Systems, Inc. 126 Ortho Development Corp. 64 Ortho Diagnostics, Inc. 24 Ortho Tec, LLC 22 Ortho Pharmaceutical Corp. 9 Ortho Source 9 Ortho Organizers, Inc. 8 Ortho Kinetics Corp. 7 Ortho Solutions Limited 6 Ortho Instruments 6 Ortho Kinematics, Inc. 6

Ortho Pared Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ortho”