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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 60 of 63

Device	Model / Reference	Registries	Class	Status
AOS TIBIAL NAIL 12mm x 45.0cm	1112-450	FDA UDI	Class II	Active
AOS CORTICAL SCREW 3.5mm x 24.0mm	S8010-240	FDA UDI	Class II	Unknown
Cannulated Headless Compression Screw, 1/2 Threaded, 3.5mm x 55mm	8081-055	FDA UDI	Class II	Active
CORTICAL SCREW DOUBLE LEAD LOCKING HEAD 3.5mm x 55mm	8114-055	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 42mm	8083-042	FDA UDI	Class II	Active
Non-Locking Screw, 4.0mm x 20mm	8085-020	FDA UDI	Class II	Active
GALILEO® LEFTY TIGHTY™ CRT²™ LAG SCREW, LEFT, 10.5mm x 125mm	1192-125	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 24mm	8001-024	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 6.5mm x 85mm	8020-085	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 28cm	S1309-028	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, RIGHT 10mm x 48cm x 130°	S1067-485	FDA UDI	Class II	Unknown
AOS THREADED CENTER PIN 6.0mm x 280mm	1161	FDA UDI	Class II	Active
Lite Semi-Tubular Plate, 15-Hole	3060-915	FDA UDI	Class II	Active
AOS ANTI-ROTATION SCREW 5.0mm x 95mm	8021-095	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 24mm	8124-024	FDA UDI	Class II	Active
Medial Pilon Plate, Right, Long, 21-Hole	3032-021	FDA UDI	Class II	Active
Medial Pilon Plate, Right, Medium, 17-Hole	3032-017	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 30mm	8124-030	FDA UDI	Class II	Active
MODULAR FLEXIBLE REAMER HEAD, Ø10.5mm	0234-105	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 12.5mm x 45cm x 130°	1123-455	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 50mm	S8061-050	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, RIGHT 10mm x 42cm x 130°	1067-425	FDA UDI	Class II	Active
AOS CORTICAL LOCKING SCREW 2.7mm x 18mm	8030-018	FDA UDI	Class II	Active
Ankle Plate Contouring Tool	9127	FDA UDI	Class I	Active
TARGETING MODULE, TROCHANTERIC NAIL 125°/20cm	1232-100	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 14mm x 45cm x 130°	S1069-455	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, LEFT 14mm x 33cm x 130°	1068-335	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 9mm x 20cm x 125°	1029-200	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 46mm	8028-046	FDA UDI	Class II	Active
Cannulatedtri-Lobe To A/O Adaptor	5018	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 45cm x 125°	S1022-455	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 13.0mm x 42cm	1013-420	FDA UDI	Class II	Active
AOS 13.5mm CANNULATED ENTRY REAMER	S0266	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 110mm	S8061-110	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 130mm	8059-130	FDA UDI	Class II	Active
CUSHING ELEVATOR FAN TIP, 15mm	0822	FDA UDI	Class I	Active
Cortical Locking Screw, 3.5mm x 30mm	8011-300	FDA UDI	Class II	Active
AOS CORTICAL TAP (AO STYLE) 2.7mm	0292	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 36cm x 130°	S1058-365	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 9.0mm x 36cm	1009-360	FDA UDI	Class II	Active
AOS MODULAR NAIL 10.0mm x 34cm	1010-340	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 80mm	8061-080	FDA UDI	Class II	Active
Ball Nose Guide Wire, Ø3.0mm x 900mm	0101-900S	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 36cm	1314-036	FDA UDI	Class II	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 100mm	8045-100	FDA UDI	Class II	Active
AOS Screw Capturing Rod, Distal Targeting Tibial Nail	0436	FDA UDI	Class I	Active
POWER CAPTURING ROD, SHORT 5.0mm	0492-100	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 42cm x 125°	S1023-425	FDA UDI	Class II	Unknown
AOS CANNULATED BLOCKING SCREW 5.0mm x 75mm	8045-075	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 65mm	8042-065	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.