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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 57 of 63

Device	Model / Reference	Registries	Class	Status
Insert Antegrade	1001	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 20mm	8012-200	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 12.5mm x 39cm x 130°	S1123-390	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 4.2mm x 40mm	S8002-040	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL, RIGHT 10mm x 39cm x 130°	1051-390	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 30cm x 130°	S1059-305	FDA UDI	Class II	Unknown
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 40mm	8042-040	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 32cm	S1318-032	FDA UDI	Class II	Unknown
AOS CANNULATED BLOCKING SCREW 5.0mm x 90mm	S8045-090	FDA UDI	Class II	Unknown
Non-Locking Screw, 4.0mm x 60mm	8085-060	FDA UDI	Class II	Active
Variable Angle Locking Screw, 2.7mm x 24mm	8087-024	FDA UDI	Class II	Active
Aos Screw Spacer/Compression Bolt	S1326	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 4.2mm x 32.5mm	8002-032	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 12.5mm x 39cm	1190-395	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 48cm	1312-048	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 48cm	S1316-048	FDA UDI	Class II	Unknown
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 60mm	8080-060	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 38cm	S1312-038	FDA UDI	Class II	Unknown
Oblique T-Plate, Left, 3 x 3-Hole	3064-006	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 26mm	8023-026	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 120mm	S8059-120	FDA UDI	Class II	Unknown
Universal Lid - Corporate Image	9940-000	FDA UDI	Class I	Active
AOS RETROGRADE FEMORAL NAIL 11mm x 36cm	1341-036	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 46mm	8024-046	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 46mm	8084-046	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 10mm x 48cm x 130°	S1051-480	FDA UDI	Class II	Unknown
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 42mm	8103-042	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 60mm	8012-600	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 55mm	8103-055	FDA UDI	Class II	Active
Slide Hammer Shaft, Galileo™ Explant	0852	FDA UDI	Class I	Active
CANNULATED LAG SCREW TAP 10.5mm	0207	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 75.0mm	8002-075	FDA UDI	Class II	Active
DRILL, Ø2.8mm	4009-200	FDA UDI	Class II	Active
AOS TIBIAL NAIL 12mm x 30.0cm	1112-300	FDA UDI	Class II	Active
Cortical Screw, 5.0mm x 46mm	8000-046	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 70mm	8103-070	FDA UDI	Class II	Active
Non-Locking Screw, 4.0mm x 32mm	8085-032	FDA UDI	Class II	Active
GALILEO® LAG SCREW, LEFT, 10.5mm x 105mm	1199-105	FDA UDI	Class II	Active
Anterolateral Distal Tibia Plate, Xxl, 31-Hole, Left	3035-031	FDA UDI	Class II	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 105mm	1045-105	FDA UDI	Class II	Active
Straight Plate, 9-Hole	3061-009	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 38mm	8001-038	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 42cm	1318-042	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 48cm	1313-048	FDA UDI	Class II	Active
AOS HUMERAL NAIL 7.0mm x 22.5cm	1171-225	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 42mm	8024-042	FDA UDI	Class II	Active
AOS TIBIAL NAIL 13mm x 30.0cm	S1113-300	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, LEFT 14mm x 39cm x 130°	1068-395	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 10mm x 20cm x 125°	1030-200	FDA UDI	Class II	Active
AOS HUMERAL NAIL 9mm x 30.0cm	S1173-300	FDA UDI	Class II	Unknown

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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.