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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 35 of 63

Device	Model / Reference	Registries	Class	Status
AOS ES™ TROCHANTERIC NAIL, LEFT 10mm x 45cm x 130°	S1066-455	FDA UDI	Class II	Unknown
Non-Locking Screw, 2.7mm x 26mm	8083-026	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 46cm	S1312-046	FDA UDI	Class II	Unknown
Implant Base Nail And Screws	9900-004	FDA UDI	Class I	Active
T-Wrench	5013	FDA UDI	Class I	Active
CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 100mm	8060-100	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 44cm	S1317-044	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 48cm	S1313-048	FDA UDI	Class II	Unknown
Calibrated Drill, AO Style, 2.0mm x 200mm	4017	FDA UDI	Class II	Active
Screw Trocar-Short Humeral Nail	0607	FDA UDI	Class I	Active
Cannulated Headless Compression Screw, 1/2 Threaded, 3.5mm x 34mm	8081-034	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 46cm	1308-046	FDA UDI	Class II	Active
Cortical Screw, 5.0mm x 44mm	8000-044	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 20mm	8023-020	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 26mm	8080-026	EUDAMEDFDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, RIGHT, Ø11mm x 30cm x 125°	1023-300	FDA UDI	Class II	Active
CORTICAL BONE SCREW 3.5mm x 20mm	8110-020	FDA UDI	Class II	Active
CORTICAL BONE SCREW 3.5mm x 38mm	8110-038	FDA UDI	Class II	Active
9/32" Hex Screwdriver, Short	0407-100	FDA UDI	Class II	Active
Aos Multi-Pin Clamp Extension One Pin	1407	FDA UDI	Class II	Active
AOS MODULAR NAIL 9.0mm x 42cm	1009-420	FDA UDI	Class II	Active
Compression Sleeve	5032-000	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 90.0mm	8002-090	FDA UDI	Class II	Active
Radiolucent Targeting Arm, Calcaneal Plate, Left, Medium	4906-040	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 65mm	8124-065	FDA UDI	Class II	Active
AOS MODULAR NAIL 9.0mm x 34cm	1009-340	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 100.0mm	8002-100	FDA UDI	Class II	Active
AOS GALILEO™ LAG SCREW, RIGHT, 10.5mm x 90mm	1099-090	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 70mm	8023-070	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 10mm x 48cm x 130°	1067-485	FDA UDI	Class II	Active
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 8mm	8031-008	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 75mm	8001-075	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 32mm	8083-032	FDA UDI	Class II	Active
MODULAR IMPLANT CASE ASSEMBLY 11, 12, 13mm	9901-102	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 55mm	S8060-055	FDA UDI	Class II	Unknown
Galileo® Capturing Rod Wrench	5048-000	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 28mm	8024-028	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 22.5mm	S8002-022	FDA UDI	Class II	Unknown
AOS CORTICAL SCREW 3.5mm x 18.0mm	S8010-180	FDA UDI	Class II	Unknown
AOS CORTICAL LOCKING SCREW 3.5mm x 34mm	8014-340	FDA UDI	Class II	Active
AOS PROXIMAL HUMERAL NAIL 8.0mm x 20cm	1170-200	FDA UDI	Class II	Active
Partially Threaded Screw, 4.0mm x 65mm	8086-065	FDA UDI	Class II	Active
AOS CANCELLOUS LAG SCREW 4.0mm x 34mm	8032-034	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 40mm	8012-400	FDA UDI	Class II	Active
AOS CLAVICLE INTRAMEDULLARY DEVICE 4.0mm x 90mm	1302-090	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 3.0mm x 100mm x 15mm	1415-100	FDA UDI	Class II	Active
Lag Screw Capturing Rod	0462-100	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 10mm x 40cm	1340-040	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 14mm x 39cm x 130°	S1069-395	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 48cm x 130°	S1058-485	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.