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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 51 of 63

Device	Model / Reference	Registries	Class	Status
Straight Plate, 13-Hole	3061-013	FDA UDI	Class II	Active
L-Plate, Left, 3 x 2-Hole	3066-005	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 40cm	1319-040	FDA UDI	Class II	Active
TARGETING MODULE, TROCHANTERIC NAIL 135°/20cm	1223	FDA UDI	Class I	Active
Pin Guide, Suprapatellar	0346	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 135mm	S8065-135	FDA UDI	Class II	Unknown
GALILEO® TROCHANTERIC NAIL, LEFT, Ø11mm x 36cm x 125°	1022-360	FDA UDI	Class II	Active
CARBON FIBER ROD, Ø9.5mm x 600mm	1152-600	FDA UDI	Class II	Active
AOS Reamer Head, 11.0mm	0204-110	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 12.5mm x 33cm x 125°	1120-335	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 10mm x 42cm x 130°	S1067-425	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL 11mm x 20cm x 130°	S1036-200	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 36cm	1311-036	FDA UDI	Class II	Active
Aos Fixation Screw Washer Retrograde Femoral Nail	1349	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 10mm x 30cm	1340-030	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 110mm	S8001-110	FDA UDI	Class II	Unknown
AOS SOLID LOCKING LAG SCREW 10.5mm x 100mm	S1094-100	FDA UDI	Class II	Unknown
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 28mm	8080-028	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 90mm	8086-090	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 105mm	8042-105	FDA UDI	Class II	Active
Impactor Pad (long)	0835	FDA UDI	Class I	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 30mm	8045-030	FDA UDI	Class II	Active
4.0mm Half Pin	4030	FDA UDI	Class II	Active
AOS Reamer Head 14.0mm	0204-140	FDA UDI	Class I	Active
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 10mm	8031-010	FDA UDI	Class II	Active
ES™ RETROGRADE FEMORAL NAIL 13mm x 30cm	1393-030	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 55mm	8084-055	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 52mm	8024-052	FDA UDI	Class II	Active
Cannulated Straight Awl W/ T-Handle	0218-100	FDA UDI	Class II	Active
AOS LAG SCREW 10.5mm x 130mm	S1045-130	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 9.0mm x 38cm	1009-380	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 125mm	S8060-125	FDA UDI	Class II	Unknown
AOS SOLID LOCKING LAG SCREW 10.5mm x 125mm	1094-125	FDA UDI	Class II	Active
Ø3.2mm PIN GUIDE, LOCKING	0312-200	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 11mm x 39cm x 130°	S1059-390	FDA UDI	Class II	Unknown
GALILEO® CRT²™ LAG SCREW, RIGHT, 10.5mm x 85mm	1092-085	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 22.5mm	8022-022	FDA UDI	Class II	Active
AOS Cannulated Entry Reamer, 16.5mm	0205	FDA UDI	Class I	Active
Aos Proximal Humeral Plate 14 Hole	3012-014	FDA UDI	Class II	Active
AOS Reamer Head, 8.0mm	0204-080	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 12mm x 34cm	1315-034	FDA UDI	Class II	Active
CORTICAL SCREW 3.5mm x 22.5mm	8010-225	FDA UDI	Class II	Active
Calibrated Step Drill (AO Style), 4.8/6.0mm	S0289	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 36cm x 130°	S1059-365	FDA UDI	Class II	Unknown
Lag Screw Inserter, Trochanteric Nail	0463	FDA UDI	Class I	Active
ES™ TROCHANTERIC NAIL, LEFT, 12.5mm x 30cm x 125 GOLD	1190-305	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 40mm	8124-040	FDA UDI	Class II	Active
VARIABLE ANGLE LOCKING SCREW, 3.5mm x 100mm	8088-100	FDA UDI	Class II	Active
Trochanteric Nail Tray, 11mm x 125˚	9902-019	FDA UDI	Class I	Active
AOS CORTICAL SCREW 3.5mm x 27.5mm	S8010-275	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.