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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 32 of 63

Device	Model / Reference	Registries	Class	Status
Clavicle Plate & Nail Set	9911-100	FDA UDI	Class I	Active
AOS LAG SCREW 10.5mm x 70mm	S1045-070	FDA UDI	Class II	Unknown
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 24mm	8100-024	FDA UDI	Class II	Active
AOS END CAP, TIBIAL NAIL 5mm	1115-050	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 22mm	8083-022	FDA UDI	Class II	Active
AOS Trocar Tip Guide Wire, 2.0mm x 300mm	0102-300	FDA UDI	Class I	Active
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 40mm	8031-040	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 22mm	8124-022	FDA UDI	Class II	Active
TARGETING MODULE, TROCHANTERIC NAIL 130°/17cm	1270-170	FDA UDI	Class I	Active
Antegrade Option, Antegrade Targeting Guide	1272	FDA UDI	Class I	Active
Targeting Arm, Left	4920-100	FDA UDI	Class II	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 90mm	8045-090	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 12.5mm x 36cm x 130°	1123-360	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 52mm	8023-052	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 75mm	8086-075	FDA UDI	Class II	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 100mm	1045-100	FDA UDI	Class II	Active
Non-Locking Screw, 2.4mm x 12mm	8082-012	FDA UDI	Class II	Active
Aos Multi-Pin Clamp Assembly Center	1406	FDA UDI	Class II	Active
Distal Tibial A-P Arm, Distal Targeting Tibial Nail	1262	FDA UDI	Class I	Active
AOS TIBIAL NAIL 10mm x 34.5cm	1110-345	FDA UDI	Class II	Active
Aos Proximal Humeral Plate 3 Hole	3012-003	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, RIGHT 11mm x 33cm x 125°	S1023-330	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 9.0mm x 30cm	1009-300	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 30mm	8028-030	FDA UDI	Class II	Active
AOS Calibrated Step Drill, 5.mm/6.5mm	0201	FDA UDI	Class I	Active
AOS TIBIAL NAIL 10mm x 30.0cm	S1110-300	FDA UDI	Class II	Unknown
Aos 95° Proximal Humeral Plate 5 Hole	3022-005	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 38cm	S1319-038	FDA UDI	Class II	Unknown
QUICK DRILL, Ø2.8mm	4027	FDA UDI	Class II	Active
Anti-Rotation And Distal Sheath, Locking	0621-100	FDA UDI	Class II	Active
Femoral Nail Instrumenst Case 1	9922	FDA UDI	Class I	Active
AOS ANTI-ROTATION SCREW 5.0mm x 85mm	8021-085	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 3.0mm x 75mm x 15mm	1415-075	FDA UDI	Class II	Active
AOS MODULAR NAIL 10.0mm x 32cm	1010-320	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 30mm	8001-030	FDA UDI	Class II	Active
DRILL GUIDE 2.9mm	0604	FDA UDI	Class I	Active
CANNULATED ENTRY REAMER, LARGE HUDSON 16.5mm	S0257	FDA UDI	Class I	Active
CANNULATED TAP 7.0mm	0241-100	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 110mm	S8065-110	FDA UDI	Class II	Unknown
Aos T10 Screwdriver, Ao Style	5008-100	FDA UDI	Class II	Active
CORTICAL SCREW DOUBLE LEAD LOCKING HEAD 3.5mm x 45mm	8114-045	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 26mm	8012-260	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 40mm	S8001-040	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 8mm x 28.5cm	S1108-285	FDA UDI	Class II	Unknown
Radiographic Ruler	0508	FDA UDI	Class I	Active
Trochanteric Nail Set 3	9978-000	FDA UDI	Class II	Active
AOS SUPRACONDYLAR FEMORAL NAIL 13mm x 18cm	1347-018	FDA UDI	Class II	Active
CANNULATED ENTRY REAMER, HUDSON 12.0mm	0228-200	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 42mm	8023-042	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 34mm	8103-034	FDA UDI	Class II	Active

Related Companies

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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.