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 24 of 63

Device	Model / Reference	Registries	Class	Status
Impactor Pad Cannulated Short	0816	FDA UDI	Class I	Active
GALILEO® TROCHANTERIC NAIL, RIGHT, Ø10mm x 45cm x 125°	1021-450	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 30cm	S1318-030	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 42cm	1314-042	FDA UDI	Class II	Active
AOS MODULAR NAIL 10.0mm x 42cm	1010-420	FDA UDI	Class II	Active
AOS CANCELLOUS TAP 3.5mm	0255	FDA UDI	Class II	Active
CANNULATED SOUND 11.0mm	0510-011	FDA UDI	Class I	Active
Anterolateral Distal Tibia Plate, Xxl, 31-Hole, Right	3036-031	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 4.2mm x 22.5mm	8002-022	FDA UDI	Class II	Active
AOS ANTI-ROTATION SCREW 5.0mm x 50mm	S8021-050	FDA UDI	Class II	Unknown
Screwdriver Handle, Cannulated	0446	FDA UDI	Class I	Active
CORTICAL BONE SCREW 3.5mm x 18mm	8110-018	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 12.5mm x 45cm x 125°	1120-455	FDA UDI	Class II	Active
Lag Screw Inserter	0463-300	FDA UDI	Class II	Active
GUIDE PIN 3.2mm x 330mm	S0100-000	FDA UDI	Class I	Active
AOS TROCHANTERIC NAIL 12mm x 17cm x 130°	S1041-170	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 44cm	S1313-044	FDA UDI	Class II	Unknown
Medial Pilon Plate, Left, Short, 13-Hole	3031-013	FDA UDI	Class II	Active
Non-Locking Screw, 2.7mm x 38mm	8083-038	FDA UDI	Class II	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 50mm	S8001-050	FDA UDI	Class II	Unknown
CORTICAL BONE SCREW 3.5mm x 26mm	8110-026	FDA UDI	Class II	Active
AOS CLAMP 5mm PIN x 5mm ROD	1400	FDA UDI	Class II	Active
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 145mm	8040-145	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 11mm x 36cm x 125°	S1022-365	FDA UDI	Class II	Unknown
AOS CANNULATED BLOCKING SCREW 5.0mm x 55mm	8045-055	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 80.0mm	8022-080	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 11mm x 42cm	S1313-042	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, RIGHT 12.5mm x 36cm x 125°	1121-365	FDA UDI	Class II	Active
AOS CLAVICLE INTRAMEDULLARY DEVICE 4.0mm x 120mm	1302-120	FDA UDI	Class II	Active
AOS PIN GUIDE 3.2mm	0335	FDA UDI	Class I	Active
AOS CAPTURED CANCELLOUS SCREW, PARTIALLY THREADED 6.0mm x 135mm	S8061-135	FDA UDI	Class II	Unknown
Plate Holding Forceps	0824-200	FDA UDI	Class I	Active
FRACTURE REDUCTION SCREWDRIVER, 3.5mm	0458-100	FDA UDI	Class II	Active
AOS END CAP, ANTEGRADE FEMORAL NAIL 0mm	S1324	FDA UDI	Class II	Unknown
PERIOSTEAL ELEVATOR SHARP, 5mm	0821	FDA UDI	Class I	Active
CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 60mm	8124-060	FDA UDI	Class II	Active
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 24mm	8031-024	FDA UDI	Class II	Active
AOS CANCELLOUS LOCKING SCREW, PARTIAL THREAD 4.0mm x 26mm	8028-026	FDA UDI	Class II	Active
AOS SOLID LOCKING LAG SCREW 10.5mm x 125mm	S1094-125	FDA UDI	Class II	Unknown
AOS SUPRACONDYLAR FEMORAL NAIL 12mm x 22cm	1346-022	FDA UDI	Class II	Active
WORKHORSE SCREW™, T10, NON-LOCKING, Ø3.5mm x 44mm	8100-044	FDA UDI	Class II	Active
Medial Pilon Plate, Left, Long, 21-Hole	3031-021	FDA UDI	Class II	Active
AOS CANCELLOUS LAG SCREW 4.0mm x 32mm	8032-032	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 46mm	8080-046	FDA UDI	Class II	Active
REAMER HEAD 10.0mm	0223-100	FDA UDI	Class I	Active
AOS MODULAR NAIL 12.0mm x 30cm	1012-300	FDA UDI	Class II	Active
Countersink	4006-000	FDA UDI	Class II	Active
AOS HUMERAL NAIL 9.0mm x 27.5cm	1173-275	FDA UDI	Class II	Active
AOS TIBIAL NAIL 9mm x 33.0cm	S1109-330	FDA UDI	Class II	Unknown
GUIDE WIRE DEPTH GAUGE 2.0mm	0515	FDA UDI	Class I	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.