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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 53 of 63

Device	Model / Reference	Registries	Class	Status
AOS HUMERAL NAIL 7mm x 27.5cm	S1171-275	FDA UDI	Class II	Unknown
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 32mm	8031-032	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 46cm	1318-046	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 10mm x 45cm x 130°	S1050-450	FDA UDI	Class II	Unknown
AOS DRILL GUIDE, GOLD 5.0mm	0320	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 14mm x 30cm x 130°	S1069-305	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 36cm	1317-036	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 50mm	S8065-050	FDA UDI	Class II	Unknown
DRILL, AO STYLE 4.0mm x 165mm	S0210-200	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 90mm	8059-090	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 150mm	8042-150	FDA UDI	Class II	Active
Tibial Nail Screw Set	9975-000	FDA UDI	Class II	Active
Multi-Pin Clamp Drill Guide	0365	FDA UDI	Class I	Unknown
AOS TROCHANTERIC NAIL, RIGHT 12.5mm x 33cm x 130°	1123-330	FDA UDI	Class II	Active
Variable Angle Locking Screw, 3.5mm x 10mm	8088-010	FDA UDI	Class II	Active
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 36mm	8031-036	FDA UDI	Class II	Active
CORTICAL BONE SCREW 3.5mm x 50mm	8110-050	FDA UDI	Class II	Active
Cortical Tap, 3.5mm, AO Style	0226-100	FDA UDI	Class I	Active
Modular Instrument Case Assembly	9901-100	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 10mm x 32cm	S1310-032	FDA UDI	Class II	Unknown
Nail Extraction Set Assembly	9925	FDA UDI	Class I	Active
Minimally Invasive Calcaneal Plate, Right, Extra Small	3077-010	FDA UDI	Class II	Active
AOS CAPTURED BULLET TIP END CAP, TROCHANTERIC NAIL 10mm	S1047-109	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 10mm x 46cm	1310-046	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 95mm	8040-095	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 12mm x 26cm	1342-026	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 50mm	8124-050	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 48mm	8001-048	FDA UDI	Class II	Active
AOS TIBIAL NAIL 13mm x 37.5cm	S1113-375	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 55mm	8061-055	FDA UDI	Class II	Active
AOS END CAP, HUMERAL NAIL 5mm	1074-050	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 2.0mm x 100mm x 15mm	1411-100	FDA UDI	Class II	Active
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 22mm	8031-022	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 75mm	S8022-075	FDA UDI	Class II	Unknown
Lag Screw Inserter	0463-200	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 42cm	1308-042	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 46cm	S1314-046	FDA UDI	Class II	Unknown
Activation Tool	0457-000	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 115mm	S8059-115	FDA UDI	Class II	Unknown
AOS HUMERAL NAIL 8mm x 20.0cm	S1172-200	FDA UDI	Class II	Unknown
REAMER HEAD 6.5mm	0223-065	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 36cm	S1317-036	FDA UDI	Class II	Unknown
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 85mm	8042-085	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 12mm x 48cm	S1315-048	FDA UDI	Class II	Unknown
AOS SOLID LOCKING LAG SCREW 10.5mm x 110mm	S1094-110	FDA UDI	Class II	Unknown
AOS A/R DRILL GUIDE 5.0mm	0302-100	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 48cm	S1309-048	FDA UDI	Class II	Unknown
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 85mm	8080-085	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 13mm x 40cm	1343-040	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 28mm	8001-028	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.