Data / Medical devices / United States / Olive Branch Distribution Center
Olive Branch Distribution Center: FDA-registered device maker in Olive Branch, MS, United States, 18 510(k) clearances and 3 PMA approvals
Olive Branch Distribution Center is registered with the FDA (registration 3016050940) in Olive Branch, MS, United States. It lists 112 device types. The FDA files 18 510(k) clearances and 3 PMA approvals under its listings, the newest dated May 21, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3016050940
- Address
- 7437 Polk Lane Suite 100, Olive Branch, MS, United States, 38654
- Owner or operator
- Highridge Medical, LLC (9061535)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- February 27, 2004
- Registered through
- 2027
- Brand names listed
- Chisel, Clamp, FlareHawk, FlareHawk Interbody Fusion System, FlareHawk11/TiHawk11, HD Lumbar Interbody System, Hive Stand-alone Anterior Lumbar Interbody System, Integrity Implants Navigated Instruments and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|
| Accessories, Photographic, For Endoscope (Exclude Light Sources) | FEM | 1 | Contract manufacturer | accessdata.fda.gov |
| Apparatus, Suction, Operating-Room, Wall Vacuum Powered | GCX | 2 | Contract manufacturer | accessdata.fda.gov |
| Appliance, Fixation, Spinal Interlaminal | KWP | 2 | Contract manufacturer, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Appliance, Fixation, Spinal Intervertebral Body | KWQ | 2 | Contract manufacturer | accessdata.fda.gov |
| Arthroscope | HRX | 2 | Contract manufacturer | accessdata.fda.gov |
| Awl | HWJ | 1 | Contract manufacturer | accessdata.fda.gov |
| Bender | HXW | 1 | Contract manufacturer | accessdata.fda.gov |
| Bit, Drill | HTW | 1 | Contract manufacturer | accessdata.fda.gov |
| Blade, Saw, General & Plastic Surgery, Surgical | GFA | 1 | Contract manufacturer | accessdata.fda.gov |
| Bone Fixation Cerclage, Sublaminar | OWI | 2 | Contract manufacturer | accessdata.fda.gov |
| Bone Grafting Material, Synthetic | LYC | 2 | Contract manufacturer | accessdata.fda.gov |
| Calcium Salt Bone Void Filler, Drillable, Non-Screw Augmentation | OIS | 2 | Contract manufacturer | accessdata.fda.gov |
| Caliper | KTZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Contract manufacturer | accessdata.fda.gov |
| Catheter And Tip, Suction | JOL | 2 | Contract manufacturer | accessdata.fda.gov |
| Ceramics, Calcium Triphosphate/Hydroxypatite, Non-Load Bearing Uses | LMN | 3 | Contract manufacturer | accessdata.fda.gov |
| Cerclage, Fixation | JDQ | 2 | Contract manufacturer | accessdata.fda.gov |
| Chisel, Surgical, Manual | FZO | 1 | Contract manufacturer | accessdata.fda.gov |
| Clamp | HXD | 1 | Contract manufacturer | accessdata.fda.gov |
| Clamp, Surgical, General & Plastic Surgery | GDJ | 1 | Contract manufacturer | accessdata.fda.gov |
| Countersink | HWW | 1 | Contract manufacturer | accessdata.fda.gov |
| Curette | HTF | 1 | Contract manufacturer | accessdata.fda.gov |
| Cutter, Surgical | FZT | 1 | Contract manufacturer | accessdata.fda.gov |
| Cutter, Wire | HXZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Dispenser, Cement | KIH | 1 | Contract manufacturer | accessdata.fda.gov |
| Dissector, Surgical, General & Plastic Surgery | GDI | 1 | Contract manufacturer | accessdata.fda.gov |
| Driver, Surgical, Pin | GFC | 1 | Contract manufacturer | accessdata.fda.gov |
| Electrosurgical Electrode Kit | NWI | 2 | Contract manufacturer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Elevator | HTE | 1 | Contract manufacturer | accessdata.fda.gov |
| Endoscope, Neurological | GWG | 2 | Contract manufacturer | accessdata.fda.gov |
| Extractor | HWB | 1 | Contract manufacturer | accessdata.fda.gov |
| File, Surgical, General & Plastic Surgery | GEO | 1 | Contract manufacturer | accessdata.fda.gov |
| Filler, Bone Void, Calcium Compound | MQV | 2 | Contract manufacturer | accessdata.fda.gov |
| Filler, Bone Void, Non-Osteoinduction | MBS | 3 | Contract manufacturer | accessdata.fda.gov |
| Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | MBP | 2 | Contract manufacturer | accessdata.fda.gov |
| Filters, Cell Collection, Tissue Processing | KET | 1 | Contract manufacturer | accessdata.fda.gov |
| Forceps | HTD | 1 | Contract manufacturer | accessdata.fda.gov |
| Forceps, General & Plastic Surgery | GEN | 1 | Contract manufacturer | accessdata.fda.gov |
| Gauge, Depth | HTJ | 1 | Contract manufacturer | accessdata.fda.gov |
| Goniometer, Nonpowered | KQW | 1 | Contract manufacturer | accessdata.fda.gov |
| Growing Rod System | PGM | 2 | Contract manufacturer | accessdata.fda.gov |
| Guide, Needle, Surgical | GDF | 1 | Contract manufacturer | accessdata.fda.gov |
| Guide, Surgical, Instrument | FZX | 1 | Contract manufacturer | accessdata.fda.gov |
| Hammer, Surgical | FZY | 1 | Contract manufacturer | accessdata.fda.gov |
| Handle, Scalpel | GDZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Hook, Bone | KIK | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hook, Surgical, General & Plastic Surgery | GDG | 1 | Contract manufacturer | accessdata.fda.gov |
| Impactor | HWA | 1 | Contract manufacturer | accessdata.fda.gov |
| Injector, Vertebroplasty (Does Not Contain Cement) | OAR | 1 | Contract manufacturer | accessdata.fda.gov |
| Instrument, Bending Or Contouring | HXP | 1 | Contract manufacturer | accessdata.fda.gov |
| Instrument, Biopsy | KNW | 2 | Contract manufacturer | accessdata.fda.gov |
| Instrument, Compression | HWN | 1 | Contract manufacturer | accessdata.fda.gov |
| Instrument, Cutting, Orthopedic | HTZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Instrument, Surgical, Non-Powered | HAO | 1 | Contract manufacturer | accessdata.fda.gov |
| Intervertebral Fusion Device With Bone Graft, Cervical | ODP | 2 | Contract manufacturer | accessdata.fda.gov |
| Intervertebral Fusion Device With Bone Graft, Lumbar | MAX | 2 | Contract manufacturer, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Intervertebral Fusion Device With Bone Graft, Thoracic | PHM | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Intervertebral Fusion Device With Integrated Fixation, Cervical | OVE | 2 | Contract manufacturer | accessdata.fda.gov |
| Intervertebral Fusion Device With Integrated Fixation, Lumbar | OVD | 2 | Contract manufacturer, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Light, Surgical, Fiberoptic | FST | 2 | Contract manufacturer | accessdata.fda.gov |
| Mallet | HXL | 1 | Contract manufacturer | accessdata.fda.gov |
| Manual Instruments Designed For Use With Total Disc Replacement Devices | QLQ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Methyl Methacrylate For Cranioplasty | GXP | 2 | Contract manufacturer | accessdata.fda.gov |
| Motor, Surgical Instrument, Ac-Powered | GEY | 1 | Contract manufacturer | accessdata.fda.gov |
| Neurological Stereotaxic Instrument | HAW | 2 | Contract manufacturer | accessdata.fda.gov |
| Orthopedic Manual Surgical Instrument | LXH | 1 | Contract manufacturer | accessdata.fda.gov |
| Orthopedic Stereotaxic Instrument | OLO | 2 | Contract manufacturer, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Orthosis, Spinal Pedicle Fixation | MNI | 2 | Contract manufacturer | accessdata.fda.gov |
| Orthosis, Spine, Plate, Laminoplasty, Metal | NQW | 2 | Contract manufacturer | accessdata.fda.gov |
| Orthosis, Spondylolisthesis Spinal Fixation | MNH | 2 | Contract manufacturer | accessdata.fda.gov |
| Osteotome | HWM | 1 | Contract manufacturer | accessdata.fda.gov |
| Osteotome, Manual | GFI | 1 | Contract manufacturer | accessdata.fda.gov |
| Passer, Wire, Orthopedic | HXI | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis | OSH | 2 | Contract manufacturer | accessdata.fda.gov |
| Plate, Fixation, Bone | HRS | 2 | Contract manufacturer | accessdata.fda.gov |
| Pliers, Surgical | HTC | 1 | Contract manufacturer | accessdata.fda.gov |
| Posterior Cervical Screw System | NKG | 2 | Contract manufacturer | accessdata.fda.gov |
| Probe | HXB | 1 | Contract manufacturer | accessdata.fda.gov |
| Prosthesis, Intervertebral Disc | MJO | 3 | Repackager or relabeler | accessdata.fda.gov |
| Punch, Surgical | LRY | 1 | Contract manufacturer | accessdata.fda.gov |
| Rasp | HTR | 1 | Contract manufacturer | accessdata.fda.gov |
| Rasp, Surgical, General & Plastic Surgery | GAC | 1 | Repackager or relabeler | accessdata.fda.gov |
| Reamer | HTO | 1 | Contract manufacturer | accessdata.fda.gov |
| Retainer, Surgical | GCZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Retractor | GAD | 1 | Contract manufacturer | accessdata.fda.gov |
| Retractor, Fiberoptic | FDG | 1 | Contract manufacturer | accessdata.fda.gov |
| Rongeur | HTX | 1 | Contract manufacturer | accessdata.fda.gov |
| Saw, Powered, And Accessories | HAB | 1 | Contract manufacturer | accessdata.fda.gov |
| Screw, Fixation, Bone | HWC | 2 | Contract manufacturer | accessdata.fda.gov |
| Screwdriver | HXX | 1 | Contract manufacturer | accessdata.fda.gov |
| Single Use Instrument Tray | OJV | 1 | Contract manufacturer | accessdata.fda.gov |
| Spatula, Orthopedic | HXR | 1 | Contract manufacturer | accessdata.fda.gov |
| Spinal Vertebral Body Replacement Device | MQP | 2 | Contract manufacturer | accessdata.fda.gov |
| Spinous Process Plate | PEK | 2 | Contract manufacturer | accessdata.fda.gov |
| Starter, Bone Screw | HWD | 1 | Contract manufacturer | accessdata.fda.gov |
| Stimulator, Bone Growth, Non-Invasive | LOF | 2 | Contract manufacturer | accessdata.fda.gov |
| Stimulator, Invasive Bone Growth | LOE | 3 | Contract manufacturer | accessdata.fda.gov |
| System, Facet Screw Spinal Device | MRW | U | Contract manufacturer | accessdata.fda.gov |
| Table And Attachments, Operating-Room | BWN | 1 | Contract manufacturer | accessdata.fda.gov |
| Tamp | HXG | 1 | Contract manufacturer | accessdata.fda.gov |
| Tap, Bone | HWX | 1 | Contract manufacturer | accessdata.fda.gov |
| Tape, Measuring, Rulers And Calipers | FTY | 1 | Contract manufacturer | accessdata.fda.gov |
| Template | HWT | 1 | Contract manufacturer | accessdata.fda.gov |
| Thoracolumbosacral Pedicle Screw System | NKB | 2 | Contract manufacturer, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Tray, Surgical | LRP | 1 | Contract manufacturer | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 1 | Contract manufacturer | accessdata.fda.gov |
| Trephine | HWK | 1 | Contract manufacturer | accessdata.fda.gov |
| Twister, Wire | HXS | 1 | Contract manufacturer | accessdata.fda.gov |
| Vertebral Body Tethering System | QHP | N | Contract manufacturer | accessdata.fda.gov |
| Wire, Fixation, Intraosseous | DZK | 2 | Contract manufacturer | accessdata.fda.gov |
| Wrench | HXC | 1 | Contract manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|
| May 21, 2025 | K243116 | FlareHawk Interbody Fusion System | MAX | Substantially Equivalent | Integrity Implants Inc. Dba Accelus | accessdata.fda.gov |
| August 7, 2023 | K231098 | LineSider® Spinal System | NKB | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| July 13, 2023 | K231769 | activL® Next Generation Instrumentation | QLQ | Substantially Equivalent | Aesculap Implants Systems, LLC | accessdata.fda.gov |
| March 25, 2022 | K213355 | Toro-L Interbody Fusion System | MAX | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| March 24, 2022 | K220453 | FlareHawk Interbody Fusion System | MAX | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| December 23, 2021 | K212088 | Integrity Implants Navigated Instruments | OLO | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| March 26, 2021 | K203038 | Toro-L Interbody Fusion System | MAX | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| December 3, 2020 | K203367 | LineSider Spinal System | NKB | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| November 3, 2020 | K202198 | FlareHawk Interbody Fusion System | MAX | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| September 23, 2020 | K201367 | FlareHawk TiHawk9 Interbody Fusion System | MAX | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| April 28, 2020 | K200541 | Hive Stand-alone Anterior Lumbar Interbody System | OVD | Substantially Equivalent | Hd Lifesciences, LLC | accessdata.fda.gov |
| June 21, 2019 | K190360 | LineSider Spinal System | NKB | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| April 3, 2019 | K183184 | FlareHawk Interbody Fusion System | MAX | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| January 7, 2019 | K182114 | FlareHawk Interbody Fusion System | MAX | Substantially Equivalent | Integrity Implants, Inc. | accessdata.fda.gov |
| July 13, 2017 | K170676 | HD Lumbar Interbody System | MAX | Substantially Equivalent | Hd Lifesciences, LLC | accessdata.fda.gov |
| October 13, 2016 | K160076 | XCage Interbody Fusion System | MAX | Substantially Equivalent | Ouroboros Medical, Inc. | accessdata.fda.gov |
| May 1, 2014 | K133514 | XCAGE INTERBODY FUSION SYSTEM | MAX | Substantially Equivalent | Ouroboros Medical | accessdata.fda.gov |
| July 28, 1981 | K811820 | BIPOLAR COAGULATING FORCEPS | GEI | Substantially Equivalent | New England Surgical Instrument Corp. | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|
| June 11, 2015 | P120024 | ACTIVL ARTIFICIAL DISC | MJO | 12 | January 29, 2026 | accessdata.fda.gov |
| August 23, 2013 | P110009 | MOBI-C CERVICAL DISC PROSTHESIS (TWO-LEVEL INDICATION) | MJO | 34 | September 16, 2026 | accessdata.fda.gov |
| August 7, 2013 | P110002 | MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION) | MJO | 34 | September 16, 2026 | accessdata.fda.gov |
Compare with other makers
Updated January 29, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.