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Orthopedic Systems, Inc.

United StatesFDA applicant, unverified

Devices
90
FDA recalls
1

Catalogue90

Newest first, rows 51-90 of 90

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  • Jackson Multipurpose Operating Table Ref K910736

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Orthopedic Drill Guide Ref K871287

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Arthroscope W/Cannulated Obtur/Drill Bits & Wrench Ref K861268

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • C Fit Cup Ref K903938

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Sagittal Knee Tester Ref K831041

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Limited Motion Functional Knee Brace Ref K831044

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • The C-S Distraction Rod Assembly Ref K890187

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Roper-Tuke Elbow Ref K873660

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Walking Heel Ref K823394

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Lead Apron Caddy Ref K870103

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Anatomic Fracture Brace Ref K823397

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Ligament Washer Ref K862991

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Freeman Modular Hip Stem Ridged Version Ref K890498

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • C-S Impactor Ref K890185

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Clark Socket, Side Rail Socket, Side Rail Section Ref K870101

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Comprehensive Spine Motion Analyzer Ref K894283

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Hyperbaric Oxygen Gurney- Ref K841368

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Sagittal & Rotary Act/Pass Knee Ligament Tester Ref K861622

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Osi Rizzoli Orthopedic Table/Manual Version Ref K880263

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Halo Traction Cervical Immobilization Ref K822885

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Drilling Template Ref K853761

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Orthopedic Lower Extremity Suspension Ref K801436

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Aesthesiometer Ref K874300

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Titanium Bone Screws Ref K874130

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Thompson Hip Prosthesis Ref K874617

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Cancellous Screw Long Thread Diameter 6.5mm Ref K895219

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bone Nail W/Washer & An Arthroscopic Insertion Sys Ref K875130

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Infant Cast Table Ref K870105

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • Bone Suture Fixation Device Ref K880264

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Arthroscopic Ankle Holder Ref K864881

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Wehbe Arm Holder Ref K880265

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Hamilton Tuckaway Desk Ref K801214

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Corin Modular Moore Stem Ref K881288

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Tendon Stripper Ref K853763

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • Osi Papoose Board Ref K864879

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • Nuffield Total Knee Ref K892503

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Isometric Acl Drill Guide Ref K853762

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Radiolucent Table Extension Ref K870104

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Tupper Trolley Ref K870102

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Femur Wrench Ref K870126

    Active Regimes: 510(k) Registry: 510(k) Class:I

Rows 51-90 of 90

Showing 51-90 of 90

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

  • 2007

    • 14 Feb 2007 Z-0780-2007 Unclassified (pre-2012) Terminated Material used to manufacture accessory bracket does not meet product specification. The screw is normally composed of ''Torlon'', which is yellow. The part was made of "Tercite", which is blue. Distribution: The products were distributed to 8 consignees in the United States, to ID, IL, NY, and CA.