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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 22 of 63

Device	Model / Reference	Registries	Class	Status
CANNULATED SOUND 9.0mm	0510-009	FDA UDI	Class I	Active
TIBIAL NAIL CASE, 12mm, 13mm	9967-000	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 40mm	8024-040	FDA UDI	Class II	Active
Variable Angle Locking Screw, 2.7mm x 36mm	8087-036	FDA UDI	Class II	Active
Calibrated Drill (AO Style), 5.5mm	S0288-200	FDA UDI	Class I	Active
Small Bone Nail Fibular Implant Set	9943-100	FDA UDI	Class I	Active
AOS CANCELLOUS SCREW 5.0mm x 95mm	S8022-095	FDA UDI	Class II	Unknown
TARGETING MODULE, TROCHANTERIC NAIL 130°/20cm	1222	FDA UDI	Class I	Active
AOS HUMERAL NAIL 9.0mm x 25cm	1173-250	FDA UDI	Class II	Active
AOS TIBIAL NAIL 10mm x 27.0cm	1110-270	FDA UDI	Class II	Active
Instrument Set 1, Trochanteric Nail System	9914-100	FDA UDI	Class II	Active
AOS Double Trocar Guide Pin, 1.5mm x 250mm	0114	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 10mm x 30cm x 130°	1066-305	FDA UDI	Class II	Active
Ratcheting Cannulated Screw Driver Handle Small Hudson	0431-100	FDA UDI	Class I	Active
Non-Locking Screw, 2.4mm x 14mm	8082-014	FDA UDI	Class II	Active
ES™ TROCHANTERIC NAIL, RIGHT, Ø11mm x 42cm x 125°	1023-425	FDA UDI	Class II	Active
LOCKING GUIDE, DISTAL TARGETING 11mm Tibial Nail	1264-011	FDA UDI	Class I	Active
Semi-Tubular Plate, 15-Hole	3060-015	FDA UDI	Class II	Active
AOS LAG SCREW 10.5mm x 140mm	S1045-140	FDA UDI	Class II	Unknown
Distal Targeting Arm, Distal Targeting Tibial Nail	1263	FDA UDI	Class I	Active
AOS CORTICAL LOCKING SCREW 2.7mm x 20mm	8030-020	FDA UDI	Class II	Active
Easy-Out Extractor, Small Hudson	0815-100	FDA UDI	Class II	Active
MODULAR FLEXIBLE REAMER HEAD, Ø13.0mm	0234-130	FDA UDI	Class II	Active
AOS HUMERAL NAIL 9.0mm x 22.5cm	1173-225	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 30cm	S1309-030	FDA UDI	Class II	Unknown
AOS CORTICAL SCREW 2.7mm x 16mm	8036-016	FDA UDI	Class II	Active
CORTICAL SCREW DOUBLE LEAD LOCKING HEAD 3.5mm x 38mm	8114-038	FDA UDI	Class II	Active
Temporary External Fixation Kit	9908-001	FDA UDI	Class II	Active
AOS TARGET CORTICAL SCREW 5.0mm x 10.0mm	8008-100	FDA UDI	Class II	Active
Compression Sleeve, Lag Screw Inserter	0465-300	FDA UDI	Class I	Active
AOS SBN ENTRY REAMER Ø6.1mm x 150mm	4019-100	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 20mm	8083-020	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 75mm	8040-075	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 36cm	S1316-036	FDA UDI	Class II	Unknown
Aos Hex Post Straight	1422	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 12.5mm x 42cm x 130°	S1122-420	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 11.0mm x 44cm	1011-440	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 75mm	8042-075	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 120mm	S8060-120	FDA UDI	Class II	Unknown
Antegrade Femoral Nail Case Right Case 1	9931	FDA UDI	Class I	Active
AOS CORTICAL SCREW 2.7mm x 36mm	8036-036	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 44cm	S1316-044	FDA UDI	Class II	Unknown
Aos End Cap, Tibial Nail Compression	1116	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 36cm	1319-036	FDA UDI	Class II	Active
AOS CANCELLOUS LAG SCREW 4.0mm x 16mm	8032-016	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 40cm	S1317-040	FDA UDI	Class II	Unknown
AOS CANNULATED BLOCKING SCREW 5.0mm x 65mm	S8045-065	FDA UDI	Class II	Unknown
AOS THREADED HALF PIN (AO STYLE) 5.0mm x 220mm x 40mm	1160-224	FDA UDI	Class II	Active
Fibonacci Lower Extremity Screw Tray	9938-000	FDA UDI	Class I	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 28mm	8028-028	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.