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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 29 of 63

Device	Model / Reference	Registries	Class	Status
AOS MODULAR NAIL 12.0mm x 42cm	1012-420	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 85mm	8041-085	FDA UDI	Class II	Active
TROCAR TIP GUIDE PIN, 3.2mm x 330mm	S0110-000	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 42cm x 130°	S1058-425	FDA UDI	Class II	Unknown
ES™ TROCHANTERIC NAIL, LEFT, Ø11mm x 30cm x 125°	1022-305	FDA UDI	Class II	Active
AOS CORTICAL LOCKING SCREW 2.7mm x 10mm	8030-010	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 85mm	8065-085	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 80mm	S8061-080	FDA UDI	Class II	Unknown
'fulpez' Driver	5000	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 45mm	S8059-045	FDA UDI	Class II	Unknown
Guide Wire Depth Gauge, Femoral Nail	0535	FDA UDI	Class I	Active
AOS TIBIAL NAIL 9mm x 30.0cm	S1109-300	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 4.2mm x 100mm	S8002-100	FDA UDI	Class II	Unknown
Ø4.0mm DISTAL DRILL GUIDE, LOCKING	0315-100	FDA UDI	Class II	Active
AOS ANTI-ROTATION SCREW 5.0mm x 70mm	8021-070	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 34mm	8012-340	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 45mm	8040-045	FDA UDI	Class II	Active
AOS Reamer Head, 15.5mm	0204-155	FDA UDI	Class I	Active
Small Bone External Fixation System Case	9933	FDA UDI	Class I	Active
AOS TIBIAL NAIL 8mm x 33.0cm	1108-330	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 10mm x 20cm x 130°	S1040-200	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 40cm	S1308-040	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 8mm x 34.5cm	S1108-345	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL, LEFT 10mm x 36cm x 130°	S1050-360	FDA UDI	Class II	Unknown
Ball Nose Guide Wire Pack Of 5	PK0103-800S	FDA UDI	Class I	Active
Bending Template, Perimeter Plate, Small	0548-020	FDA UDI	Class II	Active
Extractor Bolt Modular Nail	0801	FDA UDI	Class I	Active
Non-Locking Screw, 3.5mm x 42mm	8084-042	FDA UDI	Class II	Active
Humeral Nail Case Assembly	9903-100	FDA UDI	Class I	Active
Aos Mid-Shaft Superior Clavicle Plate Straight, Left	3005-060	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 55mm	8040-055	FDA UDI	Class II	Active
AOS CORTICAL SCREW 2.7mm x 8mm	8036-008	FDA UDI	Class II	Active
ES™ RETROGRADE FEMORAL NAIL 11mm x 38cm	1391-038	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 46cm	1312-046	FDA UDI	Class II	Active
AOS CORTICAL LOCKING SCREW 2.7mm x 12mm	8030-012	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 105mm	S8061-105	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 80mm	S8060-080	FDA UDI	Class II	Unknown
Posterior Distal Fibula Plate, Left, Short, 9-Hole	3053-009	FDA UDI	Class II	Active
Ratcheting Small Axial Handle, A-O Quick Connect, Cannulated	5026	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL, LEFT 11mm x 45cm x 130°	S1058-450	FDA UDI	Class II	Unknown
AOS CLAVICLE INTRAMEDULLARY DEVICE 4.0mm x 110mm	1302-110	FDA UDI	Class II	Active
Lite Semi-Tubular Plate, 21-Hole	3060-921	FDA UDI	Class II	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 65mm	1045-065	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 44mm	8028-044	FDA UDI	Class II	Active
Trochanteric Implant Case Assembly	9902-101	FDA UDI	Class I	Active
AOS Reamer Head, 14.5mm	0204-145	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 42cm x 130°	S1059-425	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 38cm	S1311-038	FDA UDI	Class II	Unknown
AOS CANCELLOUS SCREW 5.0mm x 37.5mm	8022-037	FDA UDI	Class II	Active
Hook Tip Depth Gauge	0531-000	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.