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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 14 of 63

Device	Model / Reference	Registries	Class	Status
AOS THREADED HALF PIN (AO STYLE) 3.0mm x 75mm x 20mm	1416-075	FDA UDI	Class II	Active
CARBON FIBER ROD, Ø9.5mm x 400mm	1152-400	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 46cm	S1308-046	FDA UDI	Class II	Unknown
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 70mm	8080-070	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 38mm	8028-038	FDA UDI	Class II	Active
AOS TIBIAL NAIL 10mm x 37.5cm	1110-375	FDA UDI	Class II	Active
AOS MODULAR NAIL 11.0mm x 34cm	1011-340	FDA UDI	Class II	Active
AOS Reamer Head, 12.5mm	0204-125	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 39cm x 125°	S1023-395	FDA UDI	Class II	Unknown
Straight Plate, 21-Hole	3061-021	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 105mm	8059-105	FDA UDI	Class II	Active
AOS TIBIAL NAIL 13mm x 39.0cm	S1113-390	FDA UDI	Class II	Unknown
Lite Semi-Tubular Plate, 19-Hole	3060-919	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 44mm	8080-044	FDA UDI	Class II	Active
AOS MODULAR NAIL 13.0mm X 36cm	1013-360	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 70mm	S8061-070	FDA UDI	Class II	Unknown
AOS CANNULATED ENTRY REAMER, LARGE HUDSON 16.5mm	0257	FDA UDI	Class I	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 14mm	8100-014	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 20.0mm	8022-020	FDA UDI	Class II	Active
Proximal Lateral Tibia Plate, Left, 14 Hole	3081-114	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 28cm	S1308-028	FDA UDI	Class II	Unknown
AOS FLOATING DRILL GUIDE 2.0/2.5mm	0330-100	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 95.0mm	8002-095	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 48mm	8103-048	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 135mm	1094-135	FDA UDI	Class II	Active
Variable Angle Locking Screw, 2.7mm x 40mm	8087-040	FDA UDI	Class II	Active
AOS Reamer Head, 9.5mm	0204-095	FDA UDI	Class I	Active
Guide Pin Depth Gauge	0506-000	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 36cm	S1308-036	FDA UDI	Class II	Unknown
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 120mm	8042-120	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 12.5mm x 30cm x 130°	1122-300	FDA UDI	Class II	Active
TROCHANTERIC NAIL TRAY, LONG, 11mm	9902-007	FDA UDI	Class I	Active
ES™ TROCHANTERIC NAIL, LEFT, Ø10mm x 36cm x 125°	1020-365	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 32cm	S1317-032	FDA UDI	Class II	Unknown
AOS 7.0mm SCREW COUNTERSINK	0262	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 33cm x 125°	S1023-335	FDA UDI	Class II	Unknown
TROCAR TIP GUIDE WIRE 2.0mm x 508mm	S0102-500	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 80mm	8065-080	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 95mm	S8001-095	FDA UDI	Class II	Unknown
GALILEO® LEFTY TIGHTY™ CRT²™ LAG SCREW, LEFT, 10.5mm x 80mm	1192-080	FDA UDI	Class II	Active
AOS SUPRACONDYLAR FEMORAL NAIL 13mm x 22cm	1347-022	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 11mm x 42cm	1341-042	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 140mm	S8065-140	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 5.0mm x 85mm	S8001-085	FDA UDI	Class II	Unknown
Non-Locking Screw, 4.0mm x 48mm	8085-048	FDA UDI	Class II	Active
CORTICAL SCREW 3.5mm x 37.5mm	8010-375	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 47.5mm	8002-047	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 12mm x 28cm	1315-028	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 130mm	8042-130	FDA UDI	Class II	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 30mm	S8045-030	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.