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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 54 of 63

Device	Model / Reference	Registries	Class	Status
Medial Pilon Plate, Xl, 25-Hole, Right	3032-025	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 42mm	8080-042	FDA UDI	Class II	Active
ES™ RETROGRADE FEMORAL NAIL 12mm x 34cm	1392-034	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 30cm	1318-030	FDA UDI	Class II	Active
Fibonacci™ Proximal Posteromedial Tibia Plate, Right, 4 Hole	3086-004	FDA UDI	Class II	Active
SOLID HEX DRIVER 2.5mm	5006	FDA UDI	Class I	Active
AOS CORTICAL SCREW 2.7mm x 26mm	8036-026	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 42cm	1319-042	FDA UDI	Class II	Active
AOS DRILL GUIDE 1.5/2.0mm	0343	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 36cm	1309-036	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 10mm x 39cm x 130°	1067-395	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 13mm x 20cm x 125°	S1033-200	FDA UDI	Class II	Unknown
AOS Cannulated Hudson Adaptor Large-Male, Small-Female	0443	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 50mm	S8002-050	FDA UDI	Class II	Unknown
AOS HEX DRIVER - LONG 3.5mm	0400-250	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 40cm	1318-040	FDA UDI	Class II	Active
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 26mm	8031-026	FDA UDI	Class II	Active
LOCKING GUIDE, DISTAL TARGETING 8mm Tibial Nail	1264-008	FDA UDI	Class I	Active
AOS HUMERAL NAIL 7mm x 32.5cm	S1171-325	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 110mm	S8059-110	FDA UDI	Class II	Unknown
AOS SOLID LOCKING LAG SCREW 10.5mm x 95mm	S1094-095	FDA UDI	Class II	Unknown
AOS DISTAL DRILL GUIDE 4.0mm	0308-100	FDA UDI	Class I	Active
AOS TIBIAL NAIL 11mm x 30.0cm	S1111-300	FDA UDI	Class II	Unknown
Non-Locking Screw, 2.4mm x 30mm	8082-030	FDA UDI	Class II	Active
AOS CORTICAL SCREW 5.0mm x 100mm	8000-100	FDA UDI	Class II	Active
MODULAR IMPLANT Case ASSEMBLY	9901-101	FDA UDI	Class I	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 45mm	8045-045	FDA UDI	Class II	Active
AOS CORTICAL TAP (AO STYLE) 3.5mm	0291	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 36cm	S1318-036	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 30cm x 125°	S1022-305	FDA UDI	Class II	Unknown
Power Driver	0408	FDA UDI	Class I	Active
AOS TIBIAL NAIL 10mm x 36.0cm	S1110-360	FDA UDI	Class II	Unknown
ES™ RETROGRADE FEMORAL NAIL 11mm x 32cm	1391-032	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 48cm	1309-048	FDA UDI	Class II	Active
Temporary Fixation Pin Compression Wheel	0832-100	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 42cm	1313-042	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 65mm	8059-065	FDA UDI	Class II	Active
Antegrade Femoral Nail Case Left Case 2	9930	FDA UDI	Class I	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 60mm	8028-060	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, LEFT, Ø10mm x 45cm x 125°	1020-450	FDA UDI	Class II	Active
GALILEO® LAG SCREW, LEFT, 10.5mm x 90mm	1199-090	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 12mm	8083-012	FDA UDI	Class II	Active
Long Universal Targeting Module	1202-100	FDA UDI	Class I	Active
T15 Driver, Hudson, Retaining	0452-400	FDA UDI	Class II	Active
CARBON FIBER ROD, Ø5.0mm x 100mm	1181-100	FDA UDI	Class II	Active
Variable Angle Locking Screw, 3.5mm x 48mm	8088-048	FDA UDI	Class II	Active
AOS LOCKING END CAP, RECON LOCK 0mm	1323	FDA UDI	Class II	Active
AOS CANCELLOUS LAG SCREW 4.0mm x 36mm	8032-036	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 38mm	8103-038	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 12mm x 36cm	1342-036	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.