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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 48 of 63

Device	Model / Reference	Registries	Class	Status
Radiolucent Targeting Arm, Calcaneal Plate, Right, Small	4907-020	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 11mm x 30cm	1341-030	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 45.0mm	8002-045	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/2 Threaded, 3.5mm x 32mm	8081-032	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 65mm	8065-065	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 46cm	1316-046	FDA UDI	Class II	Active
LITE T-PLATE, 3x3-HOLE	3063-906	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 40mm	8083-040	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 40mm	8065-040	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 125mm	8059-125	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 11mm x 42cm x 125°	S1023-420	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 40cm	S1316-040	FDA UDI	Class II	Unknown
Partially Threaded Screw, 4.0mm x 26mm	8086-026	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 33cm x 130°	1058-335	FDA UDI	Class II	Active
MODULAR FLEXIBLE REAMER HEAD, Ø10.0mm	0234-100	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 46mm	S8001-046	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 9mm x 27.0cm	1109-270	FDA UDI	Class II	Active
QUICK DRILL, Ø1.9mm	4028	FDA UDI	Class II	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 70mm	S8045-070	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL, LEFT 10mm x 48cm x 130°	S1050-480	FDA UDI	Class II	Unknown
CANNULATED SOUND 13.0mm	0510-013	FDA UDI	Class I	Active
AOS END CAP, RETROGRADE FEMORAL NAIL 5mm	1339-005	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 90mm	S8001-090	FDA UDI	Class II	Unknown
9/32 Ball Hex Driver, Large Hudson	0474-000	FDA UDI	Class II	Active
CANNULATED LEFTY TIGHTY™ CRT²™ LAG SCREW TAP, LARGE HUDSON, 10.5mm	4046-000	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 46cm	1319-046	FDA UDI	Class II	Active
AOS Drill, AO Style 3.2mm x 165mm	0229	FDA UDI	Class I	Active
Screw Gripper	5022	FDA UDI	Class I	Active
GALILEO™ LAG SCREW, RIGHT, 10.5mm x 115mm	1099-115	FDA UDI	Class II	Active
AOS CORTICAL LOCKING SCREW 3.5mm x 24mm	8014-240	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 38mm	8024-038	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, LEFT, Ø10mm x 42cm x 125°	1020-420	FDA UDI	Class II	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 46mm	8100-046	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 115mm	1094-115	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 36mm	8001-036	FDA UDI	Class II	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 20mm	8100-020	FDA UDI	Class II	Active
AOS MODULAR NAIL 12.0mm x 44cm	1012-440	FDA UDI	Class II	Active
CORTICAL BONE SCREW 3.5mm x 22mm	8110-022	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 42cm	1316-042	FDA UDI	Class II	Active
AOS TIBIAL NAIL 11mm x 37.5cm	1111-375	FDA UDI	Class II	Active
AOS MODULAR NAIL 12.0mm x 20cm	1012-200	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 38cm	S1318-038	FDA UDI	Class II	Unknown
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 145mm	8042-145	FDA UDI	Class II	Active
Cannulated Drill, Large Hudson, 5.5mm	S0232-100	FDA UDI	Class I	Active
CORTICAL SCREW 3.5mm x 22.0mm	8010-220	FDA UDI	Class II	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 100mm	8100-100	FDA UDI	Class II	Active
ES™ TROCHANTERIC NAIL, RIGHT, 12.5mm x 30cm x 125 PURPLE	1191-305	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, LEFT, Ø10mm x 36cm x 130°	1050-360	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 16mm	8084-016	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/2 Threaded, 3.5mm x 42mm	8081-042	FDA UDI	Class II	Active

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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.