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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 46 of 63

Device	Model / Reference	Registries	Class	Status
AOS SOLID LOCKING LAG SCREW 10.5mm x 85mm	1094-085	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 36mm	8023-036	FDA UDI	Class II	Active
AOS CANCELLOUS LAG SCREW 4.0mm x 22mm	8032-022	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 135mm	8061-135	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 36cm	S1309-036	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 28cm	1308-028	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 105mm	S1094-105	FDA UDI	Class II	Unknown
AOS CANCELLOUS SCREW 6.5mm x 95mm	8020-095	FDA UDI	Class II	Active
Fibonacci™ Proximal Lateral Tibia Plate, Right, 8 Hole	3082-008	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 12.5mm x 30cm x 130°	1123-305	FDA UDI	Class II	Active
Activation Tool	S0457	FDA UDI	Class I	Active
Fibonacci™ Proximal Lateral Tibia Plate, Left, 14 Hole	3081-014	FDA UDI	Class II	Active
AOS TIBIAL NAIL 13mm x 43.5cm	1113-435	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 32mm	8024-032	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 100mm	S8001-100	FDA UDI	Class II	Unknown
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 35mm	8042-035	FDA UDI	Class II	Active
Non-Locking Screw, 2.4mm x 34mm	8082-034	FDA UDI	Class II	Active
Aos Clavicle Plate, Short Lateral Superior, Right	3018	FDA UDI	Class II	Active
TROCHANTERIC NAIL TRAY ES 11mm x 125	9902-015	FDA UDI	Class I	Active
MODULAR FLEXIBLE REAMER HEAD, Ø15.0mm	0234-150	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 10mm x 17cm x 125°	S1030-170	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 30cm	S1314-030	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 85mm	S8065-085	FDA UDI	Class II	Unknown
CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 125mm	8060-125	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 11mm x 45cm x 130°	S1059-450	FDA UDI	Class II	Unknown
OBTURATOR 3.2mm	0625	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 90mm	S8060-090	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 10mm x 40cm	S1310-040	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 39cm x 125°	S1022-395	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 5.0mm x 44mm	8001-044	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 48cm	1318-048	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 18mm	8012-180	FDA UDI	Class II	Active
RADIOLUCENT TARGETING ARM 130°/17cm	1278	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 45mm	S8065-045	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 4.2mm x 42.5mm	S8002-042	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 12.0mm x 46cm	1012-460	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 70mm	S8065-070	FDA UDI	Class II	Unknown
Keyed Driver	0483	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 60mm	S8002-060	FDA UDI	Class II	Unknown
Partially Threaded Screw, 4.0mm x 44mm	8086-044	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 30mm	8012-300	FDA UDI	Class II	Active
T15 Solid Driver	0448-100	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 125mm	S8065-125	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL 9mm x 20cm x 135°	1035-200	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 40.0mm	8022-040	FDA UDI	Class II	Active
Guide Wire Depth Gauge, Tibial	0520	FDA UDI	Class I	Unknown
CALIBRATED STEP DRILL 5.0mm	S0209-200	FDA UDI	Class I	Active
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 140mm	8042-140	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 44cm	S1318-044	FDA UDI	Class II	Unknown
AOS T-Handle	0411	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.