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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 40 of 63

Device	Model / Reference	Registries	Class	Status
AOS HUMERAL NAIL 7.0mm x 27.5cm	1171-275	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 50mm	8059-050	FDA UDI	Class II	Active
AOS MODULAR NAIL 12.0mm x 25cm	1012-250	FDA UDI	Class II	Active
AOS Trocar Tip Guide Wire, 2.0mm x 150mm	0102-150	FDA UDI	Class I	Active
7.0mm TAP, SMALL HUDSON	0241-200	FDA UDI	Class II	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 75mm	1045-075	FDA UDI	Class II	Active
AOS TARGET CORTICAL SCREW 5.0mm x 15.0mm	8008-150	FDA UDI	Class II	Active
Radiolucent Targeting Arm, 125° Trochanteric Nail	1267-100	FDA UDI	Class II	Active
AOS HUMERAL NAIL 8mm x 27.5cm	S1172-275	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 10.0mm x 25cm	1010-250	FDA UDI	Class II	Active
AOS DRILL, Ø2.8mm	4009-100	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 42cm	S1309-042	FDA UDI	Class II	Unknown
OBTURATOR, Ø3.6mm	0227-000	FDA UDI	Class II	Active
4.0mm Drill Guide Multi-Pin Clamp	0364	FDA UDI	Class I	Unknown
CORTICAL SCREW 3.5mm x 17.5mm	8010-175	FDA UDI	Class II	Active
ES™ RETROGRADE FEMORAL NAIL 13mm x 40cm	1393-040	FDA UDI	Class II	Active
Bending Template, Minimally Invasive Calcaneus Plate, Large	0549-060	FDA UDI	Class II	Active
Targeter Alignment Lock	4919-000	FDA UDI	Class II	Active
T-Plate, 3 x 3-Hole	3063-006	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, Ø11mm x 20cm x 130°	1036-200	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/2 Threaded, 3.5mm x 38mm	8081-038	FDA UDI	Class II	Active
Cortical Screw, 5.0mm x 48mm	8000-048	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 46cm	S1318-046	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 45mm	S8061-045	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL, LEFT 11mm x 30cm x 130°	1058-300	FDA UDI	Class II	Active
Perimeter Calcaneal Plate, Right, Extra Small	3079-010	FDA UDI	Class II	Active
Radiographic Ruler, Antegrade/Retrograde	0532	FDA UDI	Class I	Active
Arch, Retrograde Targeting Guide	1281	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 35mm	S8059-035	FDA UDI	Class II	Unknown
AOS CORTICAL SCREW 3.5mm x 12.0mm	S8010-120	FDA UDI	Class II	Unknown
AOS CANCELLOUS SCREW 5.0mm x 70mm	S8022-070	FDA UDI	Class II	Unknown
AOS LAG SCREW 10.5mm x 105mm	S1045-105	FDA UDI	Class II	Unknown
TAP 4.3mm	4005	FDA UDI	Class I	Active
Galileo™ Extraction Instrument Case	9936	FDA UDI	Class I	Active
HEX DRIVER - SHORT 3.5mm	0417-000	FDA UDI	Class I	Active
Fibonacci™ Proximal Posteromedial Tibia Plate, Left, 8 Hole	3085-008	FDA UDI	Class II	Active
Variable Angle Locking Screw, 2.7mm x 12mm	8087-012	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 44cm	1312-044	FDA UDI	Class II	Active
AOS TIBIAL NAIL 10mm x 31.5cm	S1110-315	FDA UDI	Class II	Unknown
Reduction Tool Tibial Nail	0811	FDA UDI	Class I	Active
GALILEO® TROCHANTERIC NAIL, RIGHT, Ø11mm x 36cm x 125°	1023-360	FDA UDI	Class II	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 55mm	S8045-055	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 115mm	S8065-115	FDA UDI	Class II	Unknown
Aos Mid-Shaft Superior Clavicle Plate Straight, Right	3006-060	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 48cm x 130°	1058-485	FDA UDI	Class II	Active
AOS TIBIAL NAIL 10mm x 31.5cm	1110-315	FDA UDI	Class II	Active
ES™ TROCHANTERIC NAIL, RIGHT, Ø10mm x 39cm x 125°	1021-395	FDA UDI	Class II	Active
MONOBLOC REAMER 6.0mm	0231-060	FDA UDI	Class I	Active
AOS TIBIAL NAIL 8mm x 37.5cm	S1108-375	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 11.0mm x 32cm	1011-320	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.