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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 52 of 63

Device	Model / Reference	Registries	Class	Status
Variable Angle Locking Screw, 3.5mm x 85mm	8088-085	FDA UDI	Class II	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 115mm	1045-115	FDA UDI	Class II	Active
AOS CORTICAL SCREW 3.5mm x 32.0mm	S8010-320	FDA UDI	Class II	Unknown
Silicone Palm Handle 3/16 Square Quick Connect	0486	FDA UDI	Class I	Active
Temporary Fixation Pin, Ankle Plate	0121	FDA UDI	Class I	Active
AOS RETROGRADE FEMORAL NAIL 10mm x 44cm	1340-044	FDA UDI	Class II	Active
Locking Collet, Targeting Module Tibial Nail	1242-100	FDA UDI	Class I	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 52mm	8028-052	FDA UDI	Class II	Active
Guide Pin Depth Gauge Clavicle Im Device	0536	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 27.5mm	S8002-027	FDA UDI	Class II	Unknown
AOS PIN GUIDE 3.2mm	0319	FDA UDI	Class I	Active
REAMER HEAD 7.5mm	0223-075	FDA UDI	Class I	Active
AOS Double Round Guide Pin 1.5mm x 250mm	0115	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 37.5mm	S8002-037	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 9mm x 31.5cm	1109-315	FDA UDI	Class II	Active
Silicone Mallet	0839	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 28mm	S8001-028	FDA UDI	Class II	Unknown
Variable Angle Locking Screw, 2.7mm x 42mm	8087-042	FDA UDI	Class II	Active
ES™ RETROGRADE FEMORAL NAIL 12mm x 36cm	1392-036	FDA UDI	Class II	Active
LITE T-PLATE, 2x5-HOLE	3062-907	FDA UDI	Class II	Active
CANNULATED ENTRY REAMER 10.5mm	0221	FDA UDI	Class I	Active
Trochanteric Screw Tray	9902-002	FDA UDI	Class I	Active
AOS ANTI-ROTATION SCREW 5.0mm x 90mm	8021-090	FDA UDI	Class II	Active
Screw Sheath	0643	FDA UDI	Class I	Active
CORTICAL LOCKING SCREW 3.5mm x 32mm	8012-320	FDA UDI	Class II	Active
AOS ANTI-ROTATION SCREW 5.0mm x 110mm	8021-110	FDA UDI	Class II	Active
Lite Straight Plate, 3-Hole	3061-903	FDA UDI	Class II	Active
Trochanteric And Modular Nail Universal Lid	9900-001	FDA UDI	Class I	Active
AOS CORTICAL SCREW 3.5mm x 60.0mm	S8010-600	FDA UDI	Class II	Unknown
Non-Locking Screw, 2.7mm x 10mm	8083-010	FDA UDI	Class II	Active
AOS TIBIAL NAIL 13mm x 37.5cm	1113-375	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 22mm	S8001-022	FDA UDI	Class II	Unknown
Non-Locking Screw, 3.5mm x 34mm	8084-034	FDA UDI	Class II	Active
Variable Angle Locking Screw, 2.7mm x 30mm	8087-030	FDA UDI	Class II	Active
Expansion Kit Tray, Proximal Humeral Plate	9941-000	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 30cm	1312-030	FDA UDI	Class II	Active
GALILEO® LAG SCREW, LEFT, 10.5mm x 100mm	1199-100	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 2.0mm x 75mm x 25mm	1413-075	FDA UDI	Class II	Active
AOS TIBIAL NAIL 13mm x 33.0cm	S1113-330	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 40mm	8061-040	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, Ø11mm x 17cm x 130°	1036-170	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 95mm	S8060-095	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 9mm x 39.0cm	1109-390	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, Ø9mm x 17cm x 130°	1034-170	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 13mm x 17cm x 130°	S1037-170	FDA UDI	Class II	Unknown
Retaining T10 Driver, Short	5025-300	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 130mm	S8065-130	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 85mm	8059-085	FDA UDI	Class II	Active
Pin Guide, Suprapatellar	0346-100	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 36mm	8124-036	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.