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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 26 of 63

Device	Model / Reference	Registries	Class	Status
Non-Locking Screw, 2.4mm x 28mm	8082-028	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 12.5mm x 33cm x 130°	1123-335	FDA UDI	Class II	Active
AOS END CAP, HUMERAL NAIL 2mm	S1074-020	FDA UDI	Class II	Unknown
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 70mm	8041-070	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 48mm	8083-048	FDA UDI	Class II	Active
Jig Locking Bolt Humeral Nail	1231	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 42cm	S1314-042	FDA UDI	Class II	Unknown
AOS HUMERAL NAIL 7.0mm x 32.5cm	1171-325	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 34cm	1314-034	FDA UDI	Class II	Active
CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 95mm	8060-095	FDA UDI	Class II	Active
Impactor Pad	0826-000	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 55mm	S8061-055	FDA UDI	Class II	Unknown
AOS CANCELLOUS SCREW 5.0mm x 47.5mm	8022-047	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 9mm x 20cm x 130°	S1034-200	FDA UDI	Class II	Unknown
CORTICAL TAP 3.5mm	S0226	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL, LEFT 11mm x 30cm x 130°	S1058-300	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 32cm	S1319-032	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 130mm	S8060-130	FDA UDI	Class II	Unknown
AOS SOLID LOCKING LAG SCREW 10.5mm x 90mm	S1094-090	FDA UDI	Class II	Unknown
ES™ TROCHANTERIC NAIL, LEFT, Ø10mm x 48cm x 125°	1020-485	FDA UDI	Class II	Active
AOS MODULAR NAIL 13.0mm x 40cm	1013-400	FDA UDI	Class II	Active
TROCAR 3.2mm	0614	FDA UDI	Class I	Active
10.5mm CANNULATED ENTRY REAMER	0221-100	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 85mm	8086-085	FDA UDI	Class II	Active
AOS END CAP, HUMERAL NAIL 2mm	1074-020	FDA UDI	Class II	Active
AOS ANTI-ROTATION SCREW 5.0mm x 65mm	S8021-065	FDA UDI	Class II	Unknown
Aos Proximal Humeral Plate 11 Hole	3012-011	FDA UDI	Class II	Active
Variable Angle Locking Screw, 2.7mm x 50mm	8087-050	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 40cm	S1313-040	FDA UDI	Class II	Unknown
AOS THREADED HALF PIN (AO STYLE) 2.0mm x 100mm x 20mm	1412-100	FDA UDI	Class II	Active
AOS MODULAR NAIL 12.0mm x 32cm	1012-320	FDA UDI	Class II	Active
Locking Tool, Galileo® Lag Screw	0456-100	FDA UDI	Class II	Active
Fixed Small Axial Handle, Cannulated	5017	FDA UDI	Class I	Active
Lateral Distal Fibula Plate, Left, Short, 12-Hole	3051-012	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 42cm	1312-042	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 50mm	8084-050	FDA UDI	Class II	Active
AOS TIBIAL NAIL 8mm x 39.0cm	1108-390	FDA UDI	Class II	Active
AOS CORTICAL LOCKING SCREW 3.5mm x 55mm	8014-550	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 120mm	8001-120	FDA UDI	Class II	Active
TARGETING MODULE, TROCHANTERIC NAIL 125°/20cm	1232	FDA UDI	Class I	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 55mm	8100-055	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 20mm	8103-020	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 45mm	8061-045	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 39cm x 130°	1059-395	FDA UDI	Class II	Active
AOS CANNULATED DRILL 4.3mm x 200mm	0277-100	FDA UDI	Class I	Active
GALILEO® TROCHANTERIC NAIL, LEFT, Ø10mm x 33cm x 125°	1020-330	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 3.0mm x 55mm x 20mm	1416-055	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 42mm	8028-042	FDA UDI	Class II	Active
AOS CORTICAL SCREW 3.5mm x 17.5mm	S8010-175	FDA UDI	Class II	Unknown
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 48mm	8124-048	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.