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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 55 of 63

Device	Model / Reference	Registries	Class	Status
Non-Locking Screw, 3.5mm x 90mm	8084-090	FDA UDI	Class II	Active
AOS DRILL GUIDE 2.5mm	0327	FDA UDI	Class I	Active
AOS MODULAR NAIL 13.0mm x 38cm	1013-380	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 30mm	8024-030	FDA UDI	Class II	Active
GALILEO® LEFTY TIGHTY™ CRT²™ LAG SCREW, LEFT, 10.5mm x 115mm	1192-115	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 24mm	8028-024	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 110mm	8001-110	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 2.0mm x 55mm x 25mm	1413-055	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 140mm	S1094-140	FDA UDI	Class II	Unknown
MONOBLOC REAMER 8.5mm	0231-085	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 40.0mm	8002-040	FDA UDI	Class II	Active
AOS MODULAR NAIL 10.0mm x 36cm	1010-360	FDA UDI	Class II	Active
AOS CAPTURED END CAP WITH POST 1mm	1048-019	FDA UDI	Class II	Active
L-Plate, Right, 3 x 4-Hole	3067-007	FDA UDI	Class II	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 35mm	S8045-035	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL 13mm x 20cm x 135°	1039-200	FDA UDI	Class II	Active
AOS MONOBLOC REAMER, HUDSON, FRONT CUTTING 6.0mm	0284-060	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 90mm	S8002-090	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL, RIGHT 12.5mm x 45cm x 130°	1123-450	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 14mm x 30cm x 130°	1069-305	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 28mm	8086-028	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 6.5mm x 105mm	8020-105	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 120mm	8065-120	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 11mm x 42cm x 130°	S1058-420	FDA UDI	Class II	Unknown
Bending Template, Perimeter Calcaneal Plate, Extra Small	0548-010	FDA UDI	Class II	Active
Variable Angle Locking Screw, 3.5mm x 22mm	8088-022	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 100mm	8040-100	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 10mm x 38cm	1340-038	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 70mm	8124-070	FDA UDI	Class II	Active
Variable Angle Locking Screw, 2.7mm x 34mm	8087-034	FDA UDI	Class II	Active
Non-Locking Screw, 4.0mm x 14mm	8085-014	FDA UDI	Class II	Active
CORTICAL SCREW 3.5mm x 20.0mm	8010-200	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 80mm	8086-080	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 12.5mm x 39cm x 130°	1123-390	FDA UDI	Class II	Active
CORTICAL BONE SCREW 3.5mm x 55mm	8110-055	FDA UDI	Class II	Active
AOS LAG SCREW 10.5mm x 75mm	S1045-075	FDA UDI	Class II	Unknown
2.5mm Drill Guide, Ankle Plate	0349	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 85mm	S8060-085	FDA UDI	Class II	Unknown
CARBON FIBER ROD, Ø9.5mm x 175mm	1152-175	FDA UDI	Class II	Active
AOS GALILEO™ LAG SCREW 10.5mm x 80mm	S1099-080	FDA UDI	Class II	Unknown
AOS ANTI-ROTATION SCREW 5.0mm x 80mm	8021-080	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 60mm	8001-060	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 58mm	8023-058	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 12mm	8084-012	FDA UDI	Class II	Active
Lite Straight Plate, 9-Hole	3061-909	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 44mm	8124-044	FDA UDI	Class II	Active
Variable Angle Locking Screw, 2.7mm x 14mm	8087-014	FDA UDI	Class II	Active
Anterolateral Distal Tibia Plate, Right, Long, 23-Hole	3036-023	FDA UDI	Class II	Active
ES™ TROCHANTERIC NAIL, RIGHT, Ø11mm x 48cm x 125°	1023-485	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 85mm	S8059-085	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.