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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 8 of 63

Device	Model / Reference	Registries	Class	Status
Lite Semi-Tubular Plate, 9-Hole	3060-909	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 50mm	8001-050	FDA UDI	Class II	Active
Retrograde Guide Modular Nail	1205	FDA UDI	Class I	Active
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 90mm	8080-090	FDA UDI	Class II	Active
CARBON FIBER ROD, Ø5.0mm x 75mm	1181-075	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 42cm x 130°	1059-425	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 120mm	8041-120	FDA UDI	Class II	Active
AOS Guide Pin, 1.5 x 230mm	0109-230	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 100mm	S8065-100	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 46cm	S1311-046	FDA UDI	Class II	Unknown
Cannulated Straight Awl With T-Handle	0218-200	FDA UDI	Class II	Active
Extraction Tool	0836	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 44cm	S1311-044	FDA UDI	Class II	Unknown
Soft Tissue Protector Quick Connect	0610-100	FDA UDI	Class I	Active
ES™ TROCHANTERIC NAIL, RIGHT, Ø10mm x 30cm x 125°	1021-305	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, LEFT, Ø10mm x 39cm x 130°	1050-390	FDA UDI	Class II	Active
Screw Depth Gauge	0500	FDA UDI	Class I	Active
AOS CANCELLOUS SCREW 5.0mm x 55mm	S8022-055	FDA UDI	Class II	Unknown
Reduction Forceps, Curved, Pointed, Long Ratchet	0901	FDA UDI	Class I	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 40cm	1309-040	FDA UDI	Class II	Active
GALILEO™ LAG SCREW, RIGHT, 10.5mm x 120mm	1099-120	FDA UDI	Class II	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 42mm	8124-042	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 30mm	S8022-030	FDA UDI	Class II	Unknown
TROCHANTERIC NAIL TRAY, LONG, Ø10mm x 130°	9963-000	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 65mm	8084-065	FDA UDI	Class II	Active
Calibrated Drill (AO Style), 5.5mm	S0288-100	FDA UDI	Class I	Active
POWER HEX SCREW DRIVER 5.0mm	0488-100	FDA UDI	Class I	Active
AOS CANCELLOUS SCREW 5.0mm x 65mm	S8022-065	FDA UDI	Class II	Unknown
AOS PROXIMAL HUMERAL NAIL (EXPANDED LOCKING) 8.0mm x 15cm	1180-150	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 55mm	8080-055	FDA UDI	Class II	Active
ELEVATOR, 10mm PERIOSTEAL	0912-100	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL 11mm x 20cm x 135°	1038-200	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 90mm	S8059-090	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 9mm x 48cm	S1308-048	FDA UDI	Class II	Unknown
AOS MODULAR NAIL 12.0mm x 15cm	1012-150	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 85mm	8084-085	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 48cm	1314-048	FDA UDI	Class II	Active
Non-Locking Screw, 4.0mm x 34mm	8085-034	FDA UDI	Class II	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 70mm	8045-070	FDA UDI	Class II	Active
AOS MODULAR NAIL 11.0mm x 38cm	1011-380	FDA UDI	Class II	Active
Screw Capturing Rod, Long	0477-000	FDA UDI	Class II	Active
DRILL, AO STYLE 3.2mm x 165mm	S0229	FDA UDI	Class I	Active
Aos Cannulated Countersink	0278	FDA UDI	Class I	Active
T-Plate, 3 x 5-Hole	3063-008	FDA UDI	Class II	Active
Trochanteric Nail Tray, Short	9902-003	FDA UDI	Class I	Active
Humeral Nail Instrument Tray	9921	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL, LEFT 11mm x 33cm x 125°	S1022-330	FDA UDI	Class II	Unknown
CORTICAL TAP 5.0mm	0216	FDA UDI	Class I	Active
CORTICAL BONE SCREW 3.5mm x 28mm	8110-028	FDA UDI	Class II	Active
AOS DRILL GUIDE, NON-LOCKING/LOCKING 2.5mm	0318-100	FDA UDI	Class I	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.