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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 38 of 63

Device	Model / Reference	Registries	Class	Status
Cannulated Headless Compression Screw, 1/2 Threaded, 3.5mm x 20mm	8081-020	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 30cm	S1313-030	FDA UDI	Class II	Unknown
AOS CANNULATED TAP 5.6mm	0282	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 30cm	S1311-030	FDA UDI	Class II	Unknown
MODULAR FLEXIBLE REAMER HEAD, Ø9.0mm	0234-090	FDA UDI	Class II	Active
FLEXIBLE REAMER SHAFT 2.0mm	0222-200	FDA UDI	Class I	Active
Suture Passing Dissector	0906	FDA UDI	Class I	Active
AOS THREADED HALF PIN (AO STYLE) 5.0mm x 180mm x 20mm	1160-182	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 12mm	8014-120	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 12.5mm x 48cm x 130°	1122-485	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 52mm	8124-052	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, LEFT, Ø10mm x 33cm x 130°	1050-330	FDA UDI	Class II	Active
Cortical Screw, 5.0mm x 55mm	8000-055	FDA UDI	Class II	Active
LOCKING GUIDE, DISTAL TARGETING 13mm Tibial Nail	1264-013	FDA UDI	Class I	Active
HOHMANN RETRACTOR 15mm BLADE	0904	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 100mm	S8060-100	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 42cm	S1308-042	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 12.0mm x 40cm	1012-400	FDA UDI	Class II	Active
5.0mm Half Pin	4031	FDA UDI	Class II	Active
POWER CAPTURING ROD 5.0mm	0489-100	FDA UDI	Class I	Active
AOS TIBIAL NAIL 11mm x 36.0cm	S1111-360	FDA UDI	Class II	Unknown
Posterior Distal Tibia Plate , Right	3042-009	FDA UDI	Class II	Active
AOS ANTI-ROTATION SCREW 5.0mm x 60mm	S8021-060	FDA UDI	Class II	Unknown
Aos Proximal Humeral Plate 8 Hole	3012-008	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 11mm x 38cm	1341-038	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 48mm	8084-048	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 32cm	1314-032	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 48mm	8024-048	FDA UDI	Class II	Active
AOS TIBIAL NAIL 13mm x 34.5cm	S1113-345	FDA UDI	Class II	Unknown
AOS GALILEO™ LAG SCREW 10.5mm x 125mm	S1099-125	FDA UDI	Class II	Unknown
Lite Straight Plate, 5-Hole	3061-905	FDA UDI	Class II	Active
Minimally Invasive Calcaneal Plate, Right, Small	3077-020	FDA UDI	Class II	Active
AOS Calibrated Drill, AO Style 2.5mm x 160mm	0217-100	FDA UDI	Class I	Active
Galileo System Quick Launch Case	9917	FDA UDI	Class I	Active
Bending Iron	0823	FDA UDI	Class I	Active
AOS CANCELLOUS SCREW 6.5mm x 65mm	8020-065	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 65mm	S8002-065	FDA UDI	Class II	Unknown
Aos Lateral Superior Clavicle Plate Curved, Right	3004-020	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 12.5mm x 30cm x 130°	S1122-300	FDA UDI	Class II	Unknown
Insertion Guide Adaptor, Distal Targeting Tibial Nail	1261	FDA UDI	Class I	Active
PIN GUIDE, BLOCKING SCREW TARGETING ARM 2.0mm	1243-100	FDA UDI	Class I	Active
AOS HUMERAL NAIL 7mm x 22.5cm	S1171-225	FDA UDI	Class II	Unknown
Ratcheting Cannulated T-Handle	0430	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 46cm	S1319-046	FDA UDI	Class II	Unknown
REAMER HEAD 9.0mm	0223-090	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 80mm	8001-080	FDA UDI	Class II	Active
AOS CANCELLOUS LAG SCREW 4.0mm x 24mm	8032-024	FDA UDI	Class II	Active
AOS TIBIAL NAIL 12mm x 36.0cm	S1112-360	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL 11mm x 20cm x 125°	1031-200	FDA UDI	Class II	Active
AOS GALILEO™ LAG SCREW 10.5mm x 90mm	S1099-090	FDA UDI	Class II	Unknown

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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.