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 23 of 63

Device	Model / Reference	Registries	Class	Status
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 115mm	8040-115	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 40mm	S8065-040	FDA UDI	Class II	Unknown
Extractor Humeral Nail	0803	FDA UDI	Class I	Active
AOSCAPTURED CANCELLOUS SCREW, PARTIAL THREAD 6.0mm x 65mm	8061-065	FDA UDI	Class II	Active
GALILEO® CRT²™ LAG SCREW, RIGHT, 10.5mm x 80mm	1092-080	FDA UDI	Class II	Active
Jig Locking Bolt, Extended Humeral Nail	1231-100	FDA UDI	Class I	Active
AOS RETROGRADE FEMORAL NAIL 10mm x 34cm	1340-034	FDA UDI	Class II	Active
Double Round Guide Wire, 1.3mm x 480mm	0118-100	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 32mm	8001-032	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 14mm x 36cm	1318-036	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 65mm	S8060-065	FDA UDI	Class II	Unknown
AOS CANNULATED CANCELLOUS SCREW, 20mm THREAD 7.0mm x 70mm	8040-070	FDA UDI	Class II	Active
Cannulated Headless Compression Screw, 1/4 Threaded, 3.5mm x 48mm	8080-048	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 120mm	S8065-120	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, LEFT 12.5mm x 42cm x 130°	1122-425	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, RIGHT, Ø11mm x 48cm x 125°	1023-480	FDA UDI	Class II	Active
AOS CORTICAL SCREW 5.0mm x 75mm	8000-075	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 6.5mm x 80mm	8020-080	FDA UDI	Class II	Active
Non-Locking Screw, 3.5mm x 75mm	8084-075	FDA UDI	Class II	Active
ES™ RETROGRADE FEMORAL NAIL 13mm x 36cm	1393-036	FDA UDI	Class II	Active
CORTICAL SCREW 3.5mm x 14.0mm	8010-140	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, LEFT 12mm x 44cm	1314-044	FDA UDI	Class II	Active
Compression Sleeve, Lag Screw Inserter 130°	0465-200	FDA UDI	Class I	Active
Locking Ring	1000	FDA UDI	Class II	Active
HEX SCREW DRIVER, LARGE HUDSON 2.5mm	0452	FDA UDI	Class I	Active
AOS CAPTURED CORTICAL SCREW 5.0mm x 34mm	S8001-034	FDA UDI	Class II	Unknown
AOS ANTEGRADE FEMORAL NAIL, RIGHT 13mm x 44cm	1317-044	FDA UDI	Class II	Active
AOS CANCELLOUS SCREW 5.0mm x 45mm	S8022-045	FDA UDI	Class II	Unknown
AOS TIBIAL NAIL 12mm x 34.5cm	S1112-345	FDA UDI	Class II	Unknown
AOS THREADED HALF PIN (AO STYLE) 2.0mm x 100mm x 10mm	1410-100	FDA UDI	Class II	Active
AOS CAPTURED CANCELLOUS SCREW, FULLY THREADED 6.5mm x 60mm	S8065-060	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW 4.2mm x 80mm	S8002-080	FDA UDI	Class II	Unknown
AOS TROCHANTERIC NAIL 9mm x 20cm x 125°	S1029-200	FDA UDI	Class II	Unknown
AOS ES™ TROCHANTERIC NAIL, RIGHT 11mm x 45cm x 130°	S1059-455	FDA UDI	Class II	Unknown
Aos Spacer, Static Locking Tibial Nail	S1117	FDA UDI	Class II	Unknown
AOS CORTICAL SCREW 3.5mm x 20.0mm	S8010-200	FDA UDI	Class II	Unknown
AOS CANCELLOUS SCREW 5.0mm x 42.5mm	8022-042	FDA UDI	Class II	Active
AOS ANTEGRADE FEMORAL NAIL, RIGHT 12mm x 38cm	S1315-038	FDA UDI	Class II	Unknown
AOS SOLID LOCKING LAG SCREW 10.5mm x 90mm	1094-090	FDA UDI	Class II	Active
GALILEO® TROCHANTERIC NAIL, LEFT, Ø10mm x 36cm x 125°	1020-360	FDA UDI	Class II	Active
AOS THREADED HALF PIN (AO STYLE) 3.0mm x 55mm x 25mm	1417-055	FDA UDI	Class II	Active
AOS Cannulated Entry Reamer, Modular Nail 13.5mm	0202	FDA UDI	Class I	Active
GALILEO® LEFTY TIGHTY™ CRT²™ LAG SCREW, LEFT, 10.5mm x 100mm	1192-100	FDA UDI	Class II	Active
AOS END CAP, HUMERAL NAIL 5mm	S1074-050	FDA UDI	Class II	Unknown
AOS HUMERAL NAIL 8.0mm x 20cm	1172-200	FDA UDI	Class II	Active
TARGETING MODULE, TROCHANTERIC NAIL 120°/20cm	1234	FDA UDI	Class I	Active
Locking Knob, Insertion Guide Tibial Nail	1239-100	FDA UDI	Class I	Active
AOS THREADED HALF PIN (AO STYLE) 2.0mm x 55mm x 20mm	1412-055	FDA UDI	Class II	Active
AOS ES™ TROCHANTERIC NAIL, LEFT 10mm x 30cm x 130°	S1066-305	FDA UDI	Class II	Unknown
AOS CAPTURED CORTICAL SCREW, FULLY THREADED 6.5mm x 60mm	8059-060	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.