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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 9 of 63

Device	Model / Reference	Registries	Class	Status
AOS CANCELLOUS SCREW 5.0mm x 85.0mm	8022-085	FDA UDI	Class II	Active
Distal Sheath Humeral Nail	0602	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 140mm	S8060-140	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 80mm	8059-080	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 11mm x 34cm	S1312-034	FDA UDI	Class II	Unknown
ES™ RETROGRADE FEMORAL NAIL 12mm x 32cm	1392-032	FDA UDI	Class II	Active
AOS Guide Pin, Trocar Tip, 3.2mm x 330mm	0110-000	FDA UDI	Class I	Active
Variable Angle Locking Screw, 2.7mm x 46mm	8087-046	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 12.5mm x 48cm x 125°	1120-485	FDA UDI	Class II	Active
AOS TIBIAL NAIL 11mm x 36.0cm	1111-360	FDA UDI	Class II	Active
CARBON FIBER ROD, Ø9.5mm x 500mm	1152-500	FDA UDI	Class II	Active
HEX DRIVER, CANNULATED, LARGE HUDSON 5.0mm	0472-000	FDA UDI	Class I	Active
CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 70mm	8060-070	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 125mm	S8059-125	FDA UDI	Class II	Unknown
AOS CORTICAL SCREW 3.5mm x 40.0mm	S8010-400	FDA UDI	Class II	Unknown
AOS CANCELLOUS SCREW 5.0mm x 35mm	S8022-035	FDA UDI	Class II	Unknown
CORTICAL SCREW 3.5mm x 28.0mm	8010-280	FDA UDI	Class II	Active
AOS CANNULATED ENTRY DRILL 18.0mm	0270	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 14mm x 45cm x 130°	S1068-455	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 10mm x 48cm	1311-048	FDA UDI	Class II	Active
AOS HUMERAL NAIL 8mm x 22.5cm	S1172-225	FDA UDI	Class II	Unknown
Targeting Arm, Right	4921-100	FDA UDI	Class II	Active
AOS CALIBRATED DRILL, AO STYLE 2.0mm x 95mm	0252-100	FDA UDI	Class I	Active
AOS TIBIAL NAIL 8mm x 36.0cm	S1108-360	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 30mm	S8065-030	FDA UDI	Class II	Unknown
AOS CANNULATED BLOCKING SCREW 5.0mm x 60mm	8045-060	FDA UDI	Class II	Active
AOS SUPRACONDYLAR FEMORAL NAIL 11mm x 18cm	1345-018	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 20mm	8028-020	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 28cm	1313-028	FDA UDI	Class II	Active
Prince Tong Forceps	0909	FDA UDI	Class I	Active
T-Wrench	5009	FDA UDI	Class I	Active
CANNULATED HEX DRIVER 5.0mm	0421	FDA UDI	Class I	Active
AOS ANTI-ROTATION SCREW 5.0mm x 55mm	S8021-055	FDA UDI	Class II	Unknown
GALILEO™ LAG SCREW, RIGHT 10.5mm x 80mm	1099-080	FDA UDI	Class II	Active
Anterolateral Distal Tibia Plate, Right, Short, 15-Hole	3036-015	FDA UDI	Class II	Active
5.0mm Pin Guide Multi-Pin Clamp	0366	FDA UDI	Class I	Unknown
AOS CAPTURED CORTICAL SCREW 5.0mm x 22mm	8001-022	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 48cm	1317-048	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 46cm	1309-046	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 14mm	8103-014	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 11mm x 32cm	1341-032	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 140mm	8060-140	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 42cm x 130°	1058-425	FDA UDI	Class II	Active
AOS CORTICAL TAP, LARGE HUDSON 5.0mm	0260	FDA UDI	Class I	Active
Minimally Invasive Calcaneal Plate, Left, Large	3076-060	FDA UDI	Class II	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 135mm	1045-135	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 140mm	8059-140	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 14mm	8083-014	FDA UDI	Class II	Active
CORTICAL SCREW DOUBLE LEAD LOCKING HEAD 3.5mm x 20mm	8114-020	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 46cm	S1313-046	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.