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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 10 of 63

Device	Model / Reference	Registries	Class	Status
AOS Calibrated Step Drill, 5.0mm	0209-200	FDA UDI	Class I	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 20mm	8124-020	FDA UDI	Class II	Active
Radiolucent Insertion Guide Trochanteric Nail	1224	FDA UDI	Class I	Active
AOS RETROGRADE FEMORAL NAIL 10mm x 28cm	1340-028	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 11mm x 39cm x 130°	S1058-390	FDA UDI	Class II	Unknown
AOS CANNULATED BLOCKING SCREW 5.0mm x 100mm	S8045-100	FDA UDI	Class II	Unknown
MONOBLOC REAMER 7.0mm	0231-070	FDA UDI	Class I	Active
Flexible Reamer Shaft	0222-100	FDA UDI	Class I	Active
AOS TIBIAL NAIL 10mm x 30.0cm	1110-300	FDA UDI	Class II	Active
CARBON FIBER ROD, Ø9.5mm x 300mm	1152-300	FDA UDI	Class II	Active
ES™ RETROGRADE FEMORAL NAIL 10mm x 32cm	1390-032	FDA UDI	Class II	Active
MONOBLOC REAMER 9.5mm	0231-095	FDA UDI	Class I	Active
Non-Locking Screw, 3.5mm x 26mm	8084-026	FDA UDI	Class II	Active
AOS RETROGRADE FEMORAL NAIL 10mm x 36cm	1340-036	FDA UDI	Class II	Active
CORTICAL TAP, LARGE HUDSON 3.5mm	S0286	FDA UDI	Class I	Active
Bending Template, Perimeter Plate, Large	0548-060	FDA UDI	Class II	Active
AOS TROCHANTERIC NAIL, LEFT 11mm x 45cm x 130°	1058-450	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 135mm	S1094-135	FDA UDI	Class II	Unknown
AOS CANCELLOUS SCREW 5.0mm x 30.0mm	8022-030	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 18mm	8083-018	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 45mm	8060-045	FDA UDI	Class II	Active
Locking Collet, Targeting Module Tibial Nail	1242	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL, LEFT 12.5mm x 39cm x 130°	S1122-390	FDA UDI	Class II	Unknown
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 130mm	8060-130	FDA UDI	Class II	Active
ES™ RETROGRADE FEMORAL NAIL 10mm x 38cm	1390-038	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 30mm	S8060-030	FDA UDI	Class II	Unknown
CORTICAL BONE SCREW 3.5mm x 24mm	8110-024	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 10mm x 36cm x 130°	1066-365	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 14mm x 42cm x 130°	S1068-425	FDA UDI	Class II	Unknown
Straight Plate, 17-Hole	3061-017	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 14mm x 44cm	1319-044	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 60mm	S8060-060	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 34cm	1318-034	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 35.0mm	8022-035	FDA UDI	Class II	Active
T10 Screwdriver	5015	FDA UDI	Class I	Active
AOS CORTICAL LOCKING SCREW 2.7mm x 8mm	8030-008	FDA UDI	Class II	Active
ES™ TROCHANTERIC NAIL, RIGHT, Ø11mm x 45cm x 125°	1023-455	FDA UDI	Class II	Active
Non-Locking Screw, 2.4mm x 18mm	8082-018	FDA UDI	Class II	Active
Femoral Nail Instruments Case 2	9924	FDA UDI	Class I	Active
AOS CORTICAL SCREW 3.5mm x 22.0mm	S8010-220	FDA UDI	Class II	Unknown
Femoral Nail Screw Caddy Case	9926	FDA UDI	Class I	Active
ES™ TROCHANTERIC NAIL, LEFT, Ø11mm x 48cm x 125°	1022-485	FDA UDI	Class II	Active
AOS PROXIMAL HUMERAL NAIL 8mm x 15cm	S1170-150	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 4.2mm x 30mm	S8002-030	FDA UDI	Class II	Unknown
Screw Sheath	0615	FDA UDI	Class I	Active
AOS DRILL GUIDE 3.5mm	0331	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 90mm	8061-090	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 100.0mm	8022-100	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 36cm x 130°	1058-365	FDA UDI	Class II	Active
GALILEO® CRT²™ LAG SCREW, RIGHT, 10.5mm x 105mm	1092-105	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.