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ADVANCED ORTHOPAEDIC SOLUTIONS, INC.

Last updated May 24, 2026

What ADVANCED ORTHOPAEDIC SOLUTIONS, INC. makes

Advanced Orthopaedic Solutions, Inc. manufactures orthopaedic fixation devices, including non-bioabsorbable bone screws, femur and tibia nails, internal fixation plates and screws, and external fixation systems. Their product line also covers surgical tools such as aiming arms, reusable implantation sleeves, and reusable surgical connectors, as well as specific instruments like retractors and depth gauges.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable regulatory requirements for orthopaedic hardware.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Advanced Orthopaedic Solutions, Inc. primarily manufacture?

Advanced Orthopaedic Solutions, Inc. specializes in orthopaedic fixation devices, including non-bioabsorbable bone screws, femur and tibia nails, internal fixation systems (plates and screws), and external fixation systems. Their product line also extends to surgical tools like orthopaedic aiming arms, reusable implantation sleeves, and reusable surgical connectors, as well as specific instruments such as retractors and depth gauges. These devices are designed to support bone stabilization and fracture repair.

Where is Advanced Orthopaedic Solutions, Inc. based, and what regulatory framework does it follow?

Advanced Orthopaedic Solutions, Inc. is based in the United States. As a manufacturer, it develops devices in compliance with U.S. regulatory requirements, including those governing orthopaedic hardware. Individual devices are classified under FDA’s regulatory categories, ensuring they meet applicable standards for safety and performance.

Are Advanced Orthopaedic Solutions, Inc.’s devices listed in any regulatory registries, and if so, which ones?

Yes, Advanced Orthopaedic Solutions, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices by assigning a standardized identifier, ensuring transparency and traceability for regulatory and market surveillance purposes.

How are Advanced Orthopaedic Solutions, Inc.’s devices classified under FDA regulations?

Advanced Orthopaedic Solutions, Inc.’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional controls to ensure their safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: aosortho.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: (310) 533-9966
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 117858154

Catalogue (3113)

Page 15 of 63

Device	Model / Reference	Registries	Class	Status
GALILEO® LAG SCREW, LEFT, 10.5mm x 80mm	1199-080	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 40mm	8086-040	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 38cm	1319-038	FDA UDI	Class II	Active
Fibonacci™ Proximal Lateral Tibia Plate, Right, 11 Hole	3082-011	FDA UDI	Class II	Active
TARGETING MODULE, TROCHANTERIC NAIL 130°/17cm	1222-170	FDA UDI	Class I	Active
GALILEO® TROCHANTERIC NAIL, RIGHT, Ø11mm x 42cm x 125°	1023-420	FDA UDI	Class II	Active
AOS MODULAR NAIL 10.0mm x 15cm	1010-150	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 10mm x 36cm x 130°	S1067-365	FDA UDI	Class II	Unknown
4.0mm Drill Guide Multi-Pin Clamp	0364-100	FDA UDI	Class II	Unknown
CARBON FIBER ROD, Ø5.0mm x 125mm	1181-125	FDA UDI	Class II	Active
CORTICAL SCREW 3.5mm x 24.0mm	8010-240	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 38cm	1314-038	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 50mm	8086-050	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 12mm x 32cm	1342-032	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 46cm	1314-046	FDA UDI	Class II	Active
LARGE HUDSON SHAFT EXTENSION, 125mm	4012	FDA UDI	Class I	Active
CORTICAL SCREW 3.5mm x 27.5mm	8010-275	FDA UDI	Class II	Active
Targeting Module Humeral Nail	1228-100	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL, RIGHT 12.5mm x 30cm x 130°	1123-300	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 25mm	S8022-025	FDA UDI	Class II	Unknown
Quick Connect Coupler, Large Hudson Female, J-Hall Connect	0469-100	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 32cm	1308-032	FDA UDI	Class II	Active
AOS MODULAR NAIL 13.0mm X 44cm	1013-440	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 24mm	8024-024	FDA UDI	Class II	Active
Standard Guide Modular Nail	1206	FDA UDI	Class I	Active
Insertion Guide, Extended Tibial Nail	1240-100	FDA UDI	Class I	Active
CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 80mm	8060-080	FDA UDI	Class II	Active
Sheath Handle, Suprapatellar	0641-000	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 58mm	8024-058	FDA UDI	Class II	Active
AOS HUMERAL NAIL 8.0mm x 27.5cm	1172-275	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 85mm	8061-085	FDA UDI	Class II	Active
Proximal Lateral Tibia Plate, Left, 8 Hole	3081-108	FDA UDI	Class II	Active
AOS CORTICAL SCREW 3.5mm x 55.0mm	S8010-550	FDA UDI	Class II	Unknown
Lite Distal Hook Plate, 4-Hole	3043-904	FDA UDI	Class II	Active
Aos Clavicle Plate, Midshaft Superior 6 Hole Straight, Right	3021-060	FDA UDI	Class II	Active
Small Fragment Washer	3075	FDA UDI	Class II	Active
DRILL GUIDE, Ø2.8mm	0349-100	FDA UDI	Class I	Active
Fibonacci™ Proximal Lateral Tibia Plate, Left, 3 Hole	3081-003	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 90mm	S8022-090	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL 13mm x 20cm x 125°	1033-200	FDA UDI	Class II	Active
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 28mm	8031-028	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 130mm	S1094-130	FDA UDI	Class II	Unknown
Variable Angle Locking Screw, 3.5mm x 28mm	8088-028	FDA UDI	Class II	Active
AOS PROXIMAL HUMERAL NAIL, EXPANDED LOCKING 8mm x 15cm	S1180-150	FDA UDI	Class II	Unknown
AOS LAG SCREW 10.5mm x 135mm	S1045-135	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 100mm	S8059-100	FDA UDI	Class II	Unknown
Lite Distal Hook Plate, 6-Hole	3043-906	FDA UDI	Class II	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 28mm	8100-028	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 38mm	8086-038	FDA UDI	Class II	Active
AOS TIBIAL NAIL 13mm x 45.0cm	1113-450	FDA UDI	Class II	Active

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FDA Recalls (12)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Advanced Orthopaedic Solutions, Inc. has 12 recall records, all initiated on January 14, 2010, with each listed as terminated. The recalls were prompted by a manufacturing defect involving the short Trochanteric Nail, specifically where one component was found to be incorrectly bent. The reason cited noted that, if the issue recurred, surgery time could potentially be extended due to the need for nail exchanges.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Jan 14, 2010	Z-1182-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1190-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1188-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1187-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1186-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1184-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-118-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1191-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1189-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1183-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1181-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.
Jan 14, 2010	Z-1192-2010	—	terminated	The recall was initiated after Advanced Orthopaedic Solutions (AOS) became aware of a manufacturing defect involving the short Trochanteric Nail, where one piece was found to be incorrectly bent. If this issue were to recur, surgery time could be extended, but only slightly as nail exchanges take place commonly in a surgery of this type.