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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 13 of 63

Device	Model / Reference	Registries	Class	Status
Targeting Module, Humeral Nail	1228-200	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 55mm	8086-055	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 44mm	8023-044	FDA UDI	Class II	Active
OBTURATOR 6.0mm	0635	FDA UDI	Class I	Active
AOS CLAVICLE INTRAMEDULLARY DEVICE 4.0mm x 100mm	1302-100	FDA UDI	Class II	Active
AOS TIBIAL NAIL 10mm x 27.0cm	S1110-270	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 95mm	S8061-095	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 33cm x 130°	S1058-335	FDA UDI	Class II	Unknown
AOS CORTICAL SCREW 2.7mm x 20mm	8036-020	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 80.0mm	8002-080	FDA UDI	Class II	Active
Aos Anterior Clavicle Plate 10-Hole	3007-060	FDA UDI	Class II	Active
AOS TIBIAL NAIL 9mm x 31.5cm	S1109-315	FDA UDI	Class II	Unknown
ES™ TROCHANTERIC NAIL, LEFT, Ø10mm x 45cm x 125°	1020-455	FDA UDI	Class II	Active
DRILL, AO STYLE 2.9mm x 100mm	S0224-100	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 38cm	S1317-038	FDA UDI	Class II	Unknown
AOS CANNULATED BLOCKING SCREW 5.0mm x 50mm	S8045-050	FDA UDI	Class II	Unknown
2.5mm HEX SCREWDRIVER	0416-200	FDA UDI	Class II	Active
Variable Angle Locking Screw, 3.5mm x 90mm	8088-090	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 12.5mm x 45cm x 125°	1121-455	FDA UDI	Class II	Active
AOS TIBIAL NAIL 12mm x 31.5cm	1112-315	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 10mm x 30cm x 130°	S1051-300	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 11mm x 39.0cm	S1111-390	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 34cm	S1311-034	FDA UDI	Class II	Unknown
AOS ANTI-ROTATION SCREW 5.0mm x 100mm	8021-100	FDA UDI	Class II	Active
AOS HUMERAL NAIL 9.0mm x 30cm	1173-300	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 110mm	8040-110	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 80mm	8041-080	FDA UDI	Class II	Active
Variable Angle Locking Screw, 3.5mm x 34mm	8088-034	FDA UDI	Class II	Active
Variable Angle Locking Screw, 3.5mm x 46mm	8088-046	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, LEFT, Ø11mm x 45cm x 125°	1022-450	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 10mm x 45cm x 130°	S1067-455	FDA UDI	Class II	Unknown
Insert Retrograde/Supracondylar	1004	FDA UDI	Class II	Active
Aos Mid-Shaft Superior Clavicle Plate Curved, Right	3006-020	FDA UDI	Class II	Active
AOS TIBIAL NAIL 11mm x 34.5cm	S1111-345	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 12mm x 37.5cm	1112-375	FDA UDI	Class II	Active
Plate Holding Forceps With Window	0860	FDA UDI	Class I	Active
Lite Semi-Tubular Plate, 13-Hole	3060-913	FDA UDI	Class II	Active
CARBON FIBER ROD, Ø9.5mm x 450mm	1152-450	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 44cm	1316-044	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 5.0mm x 180mm x 30mm	1160-183	FDA UDI	Class II	Active
LITE T-PLATE, 3x5-HOLE	3063-908	FDA UDI	Class II	Active
AOS END CAP, ANTEGRADE FEMORAL NAIL 10.0mm	1322-010	FDA UDI	Class II	Active
Galileo Extraction Tool, Capturing Rod	0857-100	FDA UDI	Class II	Active
Radiolucent Targeting Arm, Calcaneal Plate, Right, Medium	4907-040	FDA UDI	Class II	Active
CALIBRATED ENTRY REAMER 5.0mm x 125mm	4000	FDA UDI	Class I	Active
GALILEO® LAG SCREW, LEFT, 10.5mm x 120mm	1199-120	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 24mm	8083-024	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 36mm	S8001-036	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 125mm	S8061-125	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 32cm	S1312-032	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.