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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 44 of 63

Device	Model / Reference	Registries	Class	Status
Lateral Distal Fibula Plate, Right, Long, 15-Hole	3052-015	FDA UDI	Class II	Active
AOS CORTICAL SCREW 2.7mm x 30mm	8036-030	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 48cm	S1312-048	FDA UDI	Class II	Unknown
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 50mm	8042-050	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 34cm	S1313-034	FDA UDI	Class II	Unknown
Variable Angle Locking Screw, 3.5mm x 70mm	8088-070	FDA UDI	Class II	Active
AOS TIBIAL NAIL 13mm x 27.0cm	1113-270	FDA UDI	Class II	Active
AOS LAG SCREW 10.5mm x 90mm	S1045-090	FDA UDI	Class II	Unknown
6.1mm Cannulated Awl	4018	FDA UDI	Class I	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 18mm	8100-018	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 3.0mm x 55mm x 10mm	1414-055	FDA UDI	Class II	Active
Slide Hammer, Galileo™ Explant	0853	FDA UDI	Class I	Active
GALILEO® TROCHANTERIC NAIL, Ø13mm x 20cm x 130°	1037-200	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 32cm	1319-032	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 110mm	S8060-110	FDA UDI	Class II	Unknown
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 46mm	8103-046	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 12mm x 44cm	1342-044	FDA UDI	Class II	Active
AOS GALILEO™ LAG SCREW 10.5mm x 105mm	S1099-105	FDA UDI	Class II	Unknown
Quick Connect Screwdriver Handle, Ao Style	0498	FDA UDI	Class I	Active
CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 75mm	8060-075	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 10mm x 33cm x 130°	1051-330	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 12mm x 20cm x 135°	1043-200	FDA UDI	Class II	Active
AOS DRILL GUIDE 2.0mm	0342	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 75mm	8061-075	FDA UDI	Class II	Active
Easyout Barrel Extractor, Galileo™ Explant	0833-100	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 12mm x 46cm	1315-046	FDA UDI	Class II	Active
Tri-Lobe To Ao Adapter, Cannulated	5018-100	FDA UDI	Class II	Active
AOS MODULAR NAIL 12.0mm x 34cm	1012-340	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 34cm	1317-034	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 32cm	1309-032	FDA UDI	Class II	Active
AOS Cannulated Drill, 2.75mm, Ankle Plate	4010-100	FDA UDI	Class II	Active
Fibonacci™ Proximal Lateral Tibia Plate, Right, 2 Hole	3082-002	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 28cm	1311-028	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 10mm x 42cm x 130°	1051-420	FDA UDI	Class II	Active
AOS CANNULATED DRILL 3.8mm x 200mm	0276-100	FDA UDI	Class I	Active
Tibial Nail 10mm x 40.5cm	1110-405	FDA UDI	Class II	Active
AOS ANTI-ROTATION SCREW 5.0mm x 75mm	8021-075	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 60.0mm	8022-060	FDA UDI	Class II	Active
Hook Tip Depth Gauge Clavicle System	0530	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 35mm	8065-035	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 44mm	8083-044	FDA UDI	Class II	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 90mm	1045-090	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 90.0mm	8022-090	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 65mm	S8065-065	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL, LEFT 11mm x 33cm x 130°	1058-330	FDA UDI	Class II	Active
POWER HEX SCREW DRIVER, SHORT 5.0mm	0491-100	FDA UDI	Class I	Active
Non-Locking Screw, 4.0mm x 30mm	8085-030	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 140mm	8040-140	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 60mm	8040-060	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 12mm x 38cm	1315-038	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.