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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 25 of 63

Device	Model / Reference	Registries	Class	Status
ES™ TROCHANTERIC NAIL TRAY, Ø14mm x 130°	9902-023	FDA UDI	Class II	Active
AOS Reamer Head, 15.0mm	0204-150	FDA UDI	Class I	Active
Proximal Lateral Tibia Plate, Right, 3 Hole	3082-103	FDA UDI	Class II	Active
Cortical Screw, 5.0mm x 90mm	8000-090	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 75mm	1094-075	FDA UDI	Class II	Active
AOS END CAP, RETROGRADE FEMORAL NAIL 1mm	1339-001	FDA UDI	Class II	Active
AOS CORTICAL SCREW 3.5mm x 16.0mm	S8010-160	FDA UDI	Class II	Unknown
Non-Locking Screw, 3.5mm x 80mm	8084-080	FDA UDI	Class II	Active
Non-Locking Screw, 4.0mm x 44mm	8085-044	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 32mm	8023-032	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 11mm x 30cm x 125°	S1023-300	FDA UDI	Class II	Unknown
Quick Connect, Large Hudson Female/ J-Hall Connect	0469	FDA UDI	Class I	Active
AOS THREADED HALF PIN (AO STYLE) 5.0mm x 220mm x 30mm	1160-223	FDA UDI	Class II	Active
AOS TIBIAL NAIL 12mm x 43.5cm	1112-435	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 13mm x 30cm	1343-030	FDA UDI	Class II	Active
CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 60mm	8060-060	FDA UDI	Class II	Active
AOS CORTICAL SCREW 3.5mm x 26.0mm	S8010-260	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, LEFT 14mm x 39cm x 130°	S1068-395	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 28cm	S1312-028	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 5.0mm x 105mm	8001-105	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 65mm	S8001-065	FDA UDI	Class II	Unknown
Reduction Bolt, Tibial Insertion Guide, Suprapatellar	1257-100	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 30mm	8061-030	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 70mm	S1094-070	FDA UDI	Class II	Unknown
Trochanteric Nail Tray ES, 10mm x 125˚	9902-017	FDA UDI	Class I	Active
Non-Locking Screw, 4.0mm x 90mm	8085-090	FDA UDI	Class II	Active
Non-Locking Screw, 2.4mm x 16mm	8082-016	FDA UDI	Class II	Active
HEX DRIVER 5.0mm	5001-000	FDA UDI	Class I	Active
AOS LAG SCREW 10.5mm x 60mm	S1045-060	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, RIGHT 12.5mm x 33cm x 125°	1121-335	FDA UDI	Class II	Active
T15 Screw Driver	0452-100	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 140mm	8065-140	FDA UDI	Class II	Active
Bone Pick 6"	0900	FDA UDI	Class I	Active
Quick Connect Screwdriver, Cannulated Silicone Handle	0453	FDA UDI	Class I	Active
ES™ RETROGRADE FEMORAL NAIL 10mm x 30cm	1390-030	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 38cm	1311-038	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 80mm	1094-080	FDA UDI	Class II	Active
AOS LAG SCREW 10.5mm x 85mm	S1045-085	FDA UDI	Class II	Unknown
Semi-Tubular Plate, 11-Hole	3060-011	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 12.5mm x 42cm x 130°	1123-425	FDA UDI	Class II	Active
AOS CORTICAL SCREW 5.0mm x 110mm	8000-110	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 50mm	S8060-050	FDA UDI	Class II	Unknown
Partially Threaded Screw, 4.0mm x 30mm	8086-030	FDA UDI	Class II	Active
AOS CALIBRATED DRILL (AO STYLE) 5.5mm	0288	FDA UDI	Class I	Active
AOS Capturing Rod, Galileo Lag screw	0455	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 75mm	S8002-075	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL 9mm x 17cm x 125°	S1029-170	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 36cm	S1311-036	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 5.0mm x 65mm	8001-065	FDA UDI	Class II	Active
AOS ANTI-ROTATION SCREW 5.0mm x 110mm	S8021-110	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.