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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 58 of 63

Device	Model / Reference	Registries	Class	Status
Drill, 1.9mm, Ankle Plate	4008	FDA UDI	Class I	Active
AOS ANTI-ROTATION SCREW 5.0mm x 105mm	S8021-105	FDA UDI	Class II	Unknown
Antegrade Targeting Module Femoral Nail System	1271-300	FDA UDI	Class I	Active
Lag Screw Sheath	0617-300	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 11mm x 20cm x 125°	S1031-200	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, LEFT 10mm x 33cm x 130°	S1066-335	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 34cm	S1319-034	FDA UDI	Class II	Unknown
AOS CANCELLOUS LOCKING SCREW 4.0mm x 60mm	8023-060	FDA UDI	Class II	Active
Tibial Insertion Guide, Extended	1255	FDA UDI	Class I	Active
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 135mm	8041-135	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 65mm	8103-065	FDA UDI	Class II	Active
AOS HUMERAL NAIL 7.0mm x 30cm	1171-300	FDA UDI	Class II	Active
Capturing Rod, Galileo® Lag Screw	5033-000	FDA UDI	Class II	Active
Distal Hook Plate, Long, 7-Hole	3043-007	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 5.0mm x 180mm x 70mm	1160-187	FDA UDI	Class II	Active
AOS CORTICAL LOCKING SCREW 3.5mm x 20mm	8014-200	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 42cm	1317-042	FDA UDI	Class II	Active
T15 Driver, Ao Style, Retaining	0432-500	FDA UDI	Class II	Active
Curved Reduction Tool	0831	FDA UDI	Class I	Active
AOS TIBIAL NAIL 12mm x 33.0cm	1112-330	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 30cm	1309-030	FDA UDI	Class II	Active
AOS CORTICAL SCREW 3.5mm x 35.0mm	S8010-350	FDA UDI	Class II	Unknown
AOS RETROGRADE FEMORAL NAIL 13mm x 42cm	1343-042	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 12.5mm x 42cm x 130°	1122-420	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 100mm	1094-100	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 95mm	S8059-095	FDA UDI	Class II	Unknown
Blocking Screw Targeting Arm	1241	FDA UDI	Class I	Active
PIN GUIDE, DISTAL TARGETING, TIBIAL NAIL 2.0mm	0619	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL 11mm x 17cm x 130°	S1036-170	FDA UDI	Class II	Unknown
Aos Clavicle Plate, Midshaft Superior 6 Hole Medium, Right	3021-040	FDA UDI	Class II	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 16mm	8100-016	FDA UDI	Class II	Active
TIBIAL NAIL 11mm x 42mm	1111-420	FDA UDI	Class II	Active
AOS FLAT WASHER 7.0mm	8039	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 36cm	S1313-036	FDA UDI	Class II	Unknown
AOS ANTI-ROTATION SCREW 5.0mm x 100mm	S8021-100	FDA UDI	Class II	Unknown
Power Lag Screw Inserter	0482	FDA UDI	Class I	Active
CANNULATED LAG SCREW TAP, LARGE HUDSON 10.5mm	S0259	FDA UDI	Class I	Active
AOS THREADED HALF PIN (AO STYLE) 3.0mm x 75mm x 25mm	1417-075	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 36mm	8028-036	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 10mm x 30cm x 130°	S1067-305	FDA UDI	Class II	Unknown
Non-Locking Screw, 4.0mm x 18mm	8085-018	FDA UDI	Class II	Active
Minimally Invasive Calcaneal Plate, Left, Medium	3076-040	FDA UDI	Class II	Active
ES Trochanteric Nail Tray, 11mm x 130°	9902-011	FDA UDI	Class I	Active
Lite Straight Plate, 17-Hole	3061-917	FDA UDI	Class II	Active
Lateral Distal Fibula Plate, Xl, 18-Hole, Right	3052-018	FDA UDI	Class II	Active
Antegrade Targeting Module Femoral Nail System	1271-100	FDA UDI	Class I	Active
AOS CANCELLOUS LAG SCREW 4.0mm x 18mm	8032-018	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 12mm x 36cm	1315-036	FDA UDI	Class II	Active
Insertion Guide Modular Nail	1200	FDA UDI	Class I	Active
Non-Locking Screw, 2.7mm x 30mm	8083-030	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.