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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 41 of 63

Device	Model / Reference	Registries	Class	Status
AOS GALILEO™ LAG SCREW 10.5mm x 115mm	S1099-115	FDA UDI	Class II	Unknown
Multi-Pin Clamp Drill Guide	0357-100	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 50mm	8065-050	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 80mm	S8001-080	FDA UDI	Class II	Unknown
Variable Angle Locking Screw, 2.7mm x 20mm	8087-020	FDA UDI	Class II	Active
Cortical Tap, AO Style, 3.5mm, Ankle Plate	4024	FDA UDI	Class I	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 50mm	8103-050	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 10mm x 39cm x 130°	S1050-390	FDA UDI	Class II	Unknown
Insertion Guide Trochanteric Nail	1220	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 10mm x 34cm	1310-034	FDA UDI	Class II	Active
AOS MODULAR NAIL 9.0mm x 40cm	1009-400	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 2.0mm x 75mm x 10mm	1410-075	FDA UDI	Class II	Active
Power Torque Limiting Adaptor, 1.7Nm	5023	FDA UDI	Class I	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 40mm	8100-040	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 65mm	8080-065	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 11mm x 36cm x 130°	1059-360	FDA UDI	Class II	Active
ES™ TROCHANTERIC NAIL, LEFT, Ø11mm x 36cm x 125°	1022-365	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 28cm	1318-028	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 10mm x 36cm x 130°	S1066-365	FDA UDI	Class II	Unknown
Calibrated Step Drill, AO Style, 4.8/6.0mm	S0289-100	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL 12mm x 17cm x 125°	S1032-170	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 9mm x 28.5cm	S1109-285	FDA UDI	Class II	Unknown
Aos Hex Bolt	1423	FDA UDI	Class II	Active
CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 65mm	8060-065	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 46mm	8083-046	FDA UDI	Class II	Active
AOS MODULAR NAIL 12.0mm x 38cm	1012-380	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 42cm	S1311-042	FDA UDI	Class II	Unknown
Compression Sleeve, Lag Screw Inserter	0465	FDA UDI	Class I	Active
GALILEO® TROCHANTERIC NAIL, RIGHT, Ø10mm x 36cm x 125°	1021-360	FDA UDI	Class II	Active
AOS CALIBRATED CORTICAL TAP 6.5mm	0272	FDA UDI	Class I	Active
Multi-Pin Clamp	1406-100	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 35mm	8060-035	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 40cm	S1318-040	FDA UDI	Class II	Unknown
AOS CANCELLOUS SCREW 6.5mm x 90mm	8020-090	FDA UDI	Class II	Active
Reduction Tool Small Bone Nail	0855-200	FDA UDI	Class I	Active
Common Instrument Base	9900-002	FDA UDI	Class I	Active
AOS MODULAR NAIL 10.0mm x 44cm	1010-440	FDA UDI	Class II	Active
Fibonacci™ Proximal Lateral Tibia Plate, Left, 2 Hole	3081-002	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 14mm x 33cm x 130°	1069-335	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 10mm	8012-100	FDA UDI	Class II	Active
Non-Locking Screw, 2.4mm x 40mm	8082-040	FDA UDI	Class II	Active
Jig Locking Bolt Modular Nail	1201	FDA UDI	Class I	Active
AOS TIBIAL NAIL 9mm x 39.0cm	S1109-390	FDA UDI	Class II	Unknown
CORTICAL TAP, LARGE HUDSON, 3.5mm	0226-200	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 100mm	8041-100	FDA UDI	Class II	Active
Fixed Axial Handle, A-O Push	0498-100	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 44mm	8103-044	FDA UDI	Class II	Active
Fibonacci Calcaneal Plate Tray	9946-100	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 12mm x 42cm	1342-042	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 10mm x 38cm	S1310-038	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.