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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 1 of 63

Device	Model / Reference	Registries	Class	Status
Targeting Module Tibial Nail	1238-100	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 10mm x 30cm x 130°	1067-305	FDA UDI	Class II	Active
Non-Locking Screw, 4.0mm x 75mm	8085-075	FDA UDI	Class II	Active
ES™ TROCHANTERIC NAIL, RIGHT, Ø11mm x 39cm x 125°	1023-395	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 14mm x 36cm x 130°	S1069-365	FDA UDI	Class II	Unknown
CORTICAL SCREW DOUBLE LEAD LOCKING HEAD 3.5mm x 50mm	8114-050	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 40mm	8028-040	FDA UDI	Class II	Active
MINI HOHMANN RETRACTOR 8mm BLADE	0903	FDA UDI	Class I	Active
TROCAR 4.0mm	0608	FDA UDI	Class I	Active
AOS TIBIAL NAIL 9mm x 28.5cm	1109-285	FDA UDI	Class II	Active
Proximal Hook Tip Depth Gauge	0507-100	FDA UDI	Class I	Active
T15 Driver (ao Style)	0432-300	FDA UDI	Class I	Active
AOS CORTICAL LOCKING SCREW 3.5mm x 36mm	8014-360	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 46cm	1313-046	FDA UDI	Class II	Active
AOS CORTICAL SCREW 3.5mm x 28.0mm	S8010-280	FDA UDI	Class II	Unknown
Medial Pilon Plate, Left, Medium, 17-Hole	3031-017	FDA UDI	Class II	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 80mm	1045-080	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 24mm	8086-024	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 44cm	1318-044	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 10mm x 42cm	1310-042	FDA UDI	Class II	Active
Reconstruction Targeting Module	1203	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 130mm	8065-130	FDA UDI	Class II	Active
AOS TIBIAL NAIL 10mm x 37.5cm	S1110-375	FDA UDI	Class II	Unknown
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 12mm	8100-012	FDA UDI	Class II	Active
ES™ TROCHANTERIC NAIL, LEFT, Ø10mm x 39cm x 125°	1020-395	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 32cm	S1309-032	FDA UDI	Class II	Unknown
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 105mm	8040-105	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 12mm x 42cm	S1315-042	FDA UDI	Class II	Unknown
AOS CAPTURED BULLET TIP END CAP, TROCHANTERIC NAIL 5mm	1047-059	FDA UDI	Class II	Active
OBTURATOR, Ø4.0mm DRILL GUIDE	0622-000	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 110mm	8065-110	FDA UDI	Class II	Active
Anterior Distal Tibia Plate, Long, 13-Hole	3039-013	FDA UDI	Class II	Active
AOS TIBIAL NAIL 12mm x 42.0cm	1112-420	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 100mm	S8022-100	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 40cm	1316-040	FDA UDI	Class II	Active
AOS PROXIMAL HUMERAL NAIL 8mm x 20cm	S1170-200	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 38cm	1308-038	FDA UDI	Class II	Active
Pin Guide, Soft Tissue Protector	0351	FDA UDI	Class I	Active
Calibrated Drill (AO Style), 5.5mm	0288-200	FDA UDI	Class I	Active
Screw Gripper	5004	FDA UDI	Class I	Active
Non-Locking Screw, 2.4mm x 20mm	8082-020	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 28cm	S1313-028	FDA UDI	Class II	Unknown
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 60mm	8100-060	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 20.0mm	8002-020	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 20mm	8084-020	FDA UDI	Class II	Active
AOS CAPTURED BULLET TIP END CAP, TROCHANTERIC NAIL 10mm	1047-109	FDA UDI	Class II	Active
22cm EXTENSION, RETROGRADE TARGETING GUIDE	1283	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL, RIGHT 11mm x 39cm x 130°	1059-390	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 85mm	8040-085	FDA UDI	Class II	Active
Lateral Distal Fibula Plate, Right, Short, 12-Hole	3052-012	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.