Is this your brand? Sign in to claim ownership.

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 37 of 63

Device	Model / Reference	Registries	Class	Status
CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 55mm	8060-055	FDA UDI	Class II	Active
Trochanteric Nail System, Case Assembly	9900-005	FDA UDI	Class I	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 10mm x 48cm x 130°	1066-485	FDA UDI	Class II	Active
Locking Targeting Arm Assembly	1291	FDA UDI	Class I	Active
Anterior Distal Tibia Plate, Short, 11-Hole	3039-011	FDA UDI	Class II	Active
CORTICAL BONE SCREW 3.5mm x 12mm	8110-012	FDA UDI	Class II	Active
Screw Driver Handle, Cannulated Silicone, Large Hudson	0467	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 120mm	8059-120	FDA UDI	Class II	Active
Lite Distal Hook Plate, 8-Hole	3043-908	FDA UDI	Class II	Active
Soft Tissue Protector, Galileo™ Explant	0640	FDA UDI	Class I	Active
AOS CANNULATED BLOCKING SCREW 5.0mm x 85mm	8045-085	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, Ø12mm x 20cm x 130°	1041-200	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW 4.0mm x 34mm	8023-034	FDA UDI	Class II	Active
CORTICAL LOCKING SCREW 3.5mm x 28mm	8012-280	FDA UDI	Class II	Active
AOS TIBIAL NAIL 8mm x 30.0cm	S1108-300	FDA UDI	Class II	Unknown
GALILEO® LEFTY TIGHTY™ CRT²™ LAG SCREW, LEFT, 10.5mm x 105mm	1192-105	FDA UDI	Class II	Active
Variable Angle Locking Screw, 3.5mm x 20mm	8088-020	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 20mm	S8022-020	FDA UDI	Class II	Unknown
AOS SOLID LOCKING LAG SCREW 10.5mm x 105mm	1094-105	FDA UDI	Class II	Active
2.7mm Calibrated Drill	4026	FDA UDI	Class II	Active
AOS CORTICAL LOCKING SCREW 3.5mm x 18mm	8014-180	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 5.0mm x 180mm x 60mm	1160-186	FDA UDI	Class II	Active
Fibonacci™ Proximal Lateral Tibia Plate, Left, 5 Hole	3081-005	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 36mm	8103-036	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 120mm	8061-120	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 45.0mm	8022-045	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 85mm	S1094-085	FDA UDI	Class II	Unknown
GALILEO® CRT²™ LAG SCREW, RIGHT, 10.5mm x 90mm	1092-090	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 55mm	8041-055	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 26mm	8103-026	FDA UDI	Class II	Active
AOS TIBIAL NAIL 8mm x 36.0cm	1108-360	FDA UDI	Class II	Active
DIAMOND WORKHORSE SCREW™, Ø3.5mm x 18mm	8103-018	FDA UDI	Class II	Active
Small Bone Nail Instrument Case	9942-100	FDA UDI	Class I	Active
LAG SCREW, 25mm THREAD LENGTH, Ø10.5mm x 85mm	1045-085	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 27.5mm	8002-027	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 32cm	1313-032	FDA UDI	Class II	Active
AOS END CAP, TIBIAL NAIL 10mm	1115-100	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 95mm	8061-095	FDA UDI	Class II	Active
REAMER HEAD 7.0mm	0223-070	FDA UDI	Class I	Active
AOS DRILL GUIDE 4.0mm	0337	FDA UDI	Class I	Active
AOS FLOATING DRILL GUIDE 2.5mm	0330	FDA UDI	Class I	Active
T10 Screwdriver, Solid	5020	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 46cm	S1317-046	FDA UDI	Class II	Unknown
Non-Locking Screw, 2.4mm x 10mm	8082-010	FDA UDI	Class II	Active
Anterolateral Distal Tibia Plate, Left, Short, 15-Hole	3035-015	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 46cm	S1309-046	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 12mm x 28.5cm	S1112-285	FDA UDI	Class II	Unknown
Alignment Guide 95° Php	1288	FDA UDI	Class I	Active
Wrench, External Fixation	1153	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL, RIGHT 11mm x 45cm x 130°	1059-450	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.