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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 43 of 63

Device	Model / Reference	Registries	Class	Status
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 110mm	8042-110	FDA UDI	Class II	Active
AOS GALILEO™ LAG SCREW 10.5mm x 95mm	S1099-095	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 10.0mm x 46cm	1010-460	FDA UDI	Class II	Active
Radiolucent Targeting Arm, Calcaneal, Left, Extra Small	4906-010	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 42cm	S1316-042	FDA UDI	Class II	Unknown
TROCHANTERIC NAIL TRAY, LONG, Ø11mm x 125°	9961-000	FDA UDI	Class II	Active
AOS Guide Wire Obturator, 3.0mm x 520mm	0104	FDA UDI	Class I	Active
AOS TIBIAL NAIL 12mm x 28.5cm	1112-285	FDA UDI	Class II	Active
Soft Tissue Protector, Hudson Quick Connect	0623-000	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 39cm x 130°	S1058-395	FDA UDI	Class II	Unknown
Ø5.0mm ANTI-ROTATION DRILL GUIDE, LOCKING	0313-100	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL RIGHT, 12.5mm x 39cm	1191-395	FDA UDI	Class II	Active
AOS TIBIAL NAIL 8mm x 27.0cm	1108-270	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 12.5mm x 33cm x 130°	1122-335	FDA UDI	Class II	Active
AOS HUMERAL NAIL 8mm x 25.0cm	S1172-250	FDA UDI	Class II	Unknown
Fibonacci Lower Extremity Instrument Tray	9937-000	FDA UDI	Class I	Active
AOS Drill, 2.0mm x 95mm	0249	FDA UDI	Class I	Active
AOS CLAVICLE INTRAMEDULLARY DEVICE 3.5mm x 120mm	1300-120	FDA UDI	Class II	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 130mm	1045-130	FDA UDI	Class II	Active
Ball Nose Guide Wire Pack Of 10	PK0101-900S	FDA UDI	Class I	Active
ES™ TROCHANTERIC NAIL, LEFT, Ø10mm x 42cm x 125°	1020-425	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 130mm	8061-130	FDA UDI	Class II	Active
ENTRY TUBE 12.5mm	0612	FDA UDI	Class I	Active
AOS CORTICAL SCREW 3.5mm x 10.0mm	8010-100	FDA UDI	Class II	Active
AOS CANCELLOUS LAG SCREW 4.0mm x 26mm	8032-026	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 44cm	1311-044	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 40mm	8023-040	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 120mm	S8001-120	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 55mm	8065-055	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 45mm	8012-450	FDA UDI	Class II	Active
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 38mm	8031-038	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 30cm	1314-030	FDA UDI	Class II	Active
3.5mm Cortical Tap (ao Style)	4024-100	FDA UDI	Class I	Active
Non-Locking Screw, 3.5mm x 38mm	8084-038	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 11mm x 28cm	1341-028	FDA UDI	Class II	Active
Non-Locking Screw, 4.0mm x 22mm	8085-022	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 90mm	8001-090	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 48cm	1319-048	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 11mm x 20cm x 120°	1082-200	FDA UDI	Class II	Active
AOS LAG SCREW 10.5mm x 110mm	S1045-110	FDA UDI	Class II	Unknown
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 32mm	8124-032	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 115mm	8001-115	FDA UDI	Class II	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 70mm	8100-070	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 3.0mm x 55mm x 15mm	1415-055	FDA UDI	Class II	Active
Locking Tool, Galileo™ Lag Screw	0456	FDA UDI	Class I	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 40mm	8045-040	FDA UDI	Class II	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 95mm	S8045-095	FDA UDI	Class II	Unknown
Small Bone External Fixation System Case	9933-100	FDA UDI	Class II	Active
Screw Depth Gauge Humeral Nail	0513-100	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 44cm	S1312-044	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.