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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 59 of 63

Device	Model / Reference	Registries	Class	Status
AOS CAPTURED CORTICAL SCREW 4.2mm x 35.0mm	8002-035	FDA UDI	Class II	Active
Minimally Invasive Calcaneal Plate, Right, Large	3077-060	FDA UDI	Class II	Active
Lite Straight Plate, 15-Hole	3061-915	FDA UDI	Class II	Active
AOS HUMERAL NAIL 7.0mm x 20cm	1171-200	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 10mm	8103-010	FDA UDI	Class II	Active
Ratcheting Comfort Cannulated T-Handle Small Hudson Adapter	0430-100	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 10mm x 39cm x 130°	1066-395	FDA UDI	Class II	Active
Cannulated Screw Depth Gauge	0517	FDA UDI	Class I	Active
Adjustable Stop	0261-000	FDA UDI	Class II	Active
Fibonacci™ Proximal Lateral Tibia Plate, Right, 14 Hole	3082-014	FDA UDI	Class II	Active
Drill Pin Depth Gauge, Ankle Plate	0541	FDA UDI	Class I	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 50mm	8023-050	FDA UDI	Class II	Active
Fibonacci™ Proximal Lateral Tibia Plate, Left, 8 Hole	3081-008	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 35mm	8061-035	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 42cm	S1318-042	FDA UDI	Class II	Unknown
LID, 3.5mm SCREW CADDY	9912-007	FDA UDI	Class II	Active
Humeral Nail Case Assembly	9903-200	FDA UDI	Class I	Active
MINI TRAY, 1.5 x 2.7 x 1.0	9907-000	FDA UDI	Class II	Active
Non-Locking Screw, 4.0mm x 85mm	8085-085	FDA UDI	Class II	Active
Proximal Lateral Tibia Plate, Left, 2 Hole	3081-102	FDA UDI	Class II	Active
GUIDE PIN DEPTH GAUGE For 15 Inch Guide Pin Only	0524	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL, RIGHT 10mm x 39cm x 130°	S1051-390	FDA UDI	Class II	Unknown
Non-Locking Screw, 4.0mm x 16mm	8085-016	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 12mm x 32cm	1315-032	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 2.0mm x 100mm x 25mm	1413-100	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 38mm	8080-038	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 28cm	1309-028	FDA UDI	Class II	Active
Bending Template, Perimeter Plate, Medium	0548-040	FDA UDI	Class II	Active
CALIBRATED DRILL 1.5mm x 110mm	4001	FDA UDI	Class I	Active
AOS MODULAR NAIL 10.0mm x 30cm	1010-300	FDA UDI	Class II	Active
Captured T10 Screwdriver	5015-200	FDA UDI	Class II	Active
Drill, 2.5mm, Ankle Plate	4009	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 10mm x 48cm	S1310-048	FDA UDI	Class II	Unknown
AOS CANNULATED DRILL 4.0mm x 200mm	0277	FDA UDI	Class I	Active
Clavicle Elevator	0842	FDA UDI	Class I	Active
Variable Angle Locking Screw, 3.5mm x 60mm	8088-060	FDA UDI	Class II	Active
ES™ TROCHANTERIC NAIL TRAY, Ø12.5mm x 125°	9902-020	FDA UDI	Class II	Active
Trochanteric Nail Set 2	9977-000	FDA UDI	Class II	Active
AOS Cannulated Drill, Large Hudson 5.5mm	0232-100	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 36cm x 125°	S1023-365	FDA UDI	Class II	Unknown
CORTICAL SCREW 3.5mm x 50.0mm	8010-500	FDA UDI	Class II	Active
2.0mm Calibrated Drill, AO Style	0252	FDA UDI	Class I	Active
Soft Tissue Protector Hudson Quick Connect	0634-100	FDA UDI	Class I	Active
AOS TIBIAL NAIL 12mm x 39.0cm	S1112-390	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 44cm	S1319-044	FDA UDI	Class II	Unknown
Aos Mid-Shaft Superior Clavicle Plate Curved, Left	3005-020	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 32cm	S1316-032	FDA UDI	Class II	Unknown
Variable Angle Locking Screw, 3.5mm x 38mm	8088-038	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 12.5mm x 45cm x 130°	1122-450	FDA UDI	Class II	Active
AOS Drill, AO Style, 2.9mm x 100mm	0224-100	FDA UDI	Class I	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.