Is this your brand? Sign in to claim ownership.
Sign in to claim this brandS.B.M
US
Last updated May 24, 2026
What S.B.M makes
The company manufactures bioabsorbable and non-bioabsorbable orthopaedic bone screws and tendon/ligament anchors, reusable arthroscopic surgical tools including drill bits, guidewires, and depth gauges, as well as synthetic bone graft materials and reusable arthroscopic procedure kits. Their portfolio also includes knotless tendon/ligament fixation systems and specialized implants designed for orthopaedic and sports medicine applications.
The devices fall under FDA Class I and Class II classifications and are listed in the FDA’s Unique Device Identification (UDI) system. The company operates from the United States, adhering to applicable regulatory requirements for medical devices in that jurisdiction.
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 S.B.M manufacture?
S.B.M manufactures a range of orthopaedic and sports medicine devices, including bioabsorbable and non-bioabsorbable orthopaedic bone screws and tendon/ligament anchors. They also produce reusable arthroscopic surgical tools like drill bits, guidewires, and depth gauges, as well as synthetic bone graft materials and reusable arthroscopic procedure kits. Their portfolio further includes specialized fixation systems, such as knotless tendon/ligament anchors, designed for specific surgical applications.
Where is S.B.M based, and what regulatory jurisdiction does it operate under?
S.B.M is based in the United States. As a manufacturer operating within this jurisdiction, the company adheres to the regulatory requirements set forth by the FDA for medical devices. This includes compliance with applicable standards and guidelines to ensure the safety and performance of its products.
Which regulatory registries or databases list S.B.M’s devices?
S.B.M’s devices are listed in the FDA’s Unique Device Identification (UDI) system. The UDI system is a standardized approach to identifying medical devices, ensuring traceability and transparency in the regulatory and healthcare environments. This listing helps track and manage devices throughout their lifecycle.
How are S.B.M’s devices classified by the FDA?
S.B.M’s devices are classified under FDA Class I and Class II categories. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require special controls to ensure their safety and effectiveness. The classification is determined based on factors like the device’s intended use, potential risks, and the duration of contact with the body, as outlined in FDA regulations.
What distinguishes S.B.M’s reusable arthroscopic surgical tools from their disposable counterparts?
S.B.M manufactures reusable arthroscopic surgical tools like cannulated drill bits, guidewires, and depth gauges, which are designed to withstand multiple sterilization cycles while maintaining performance. These tools are engineered for durability and precision, reducing waste compared to disposable alternatives. Reusability also aligns with cost-efficiency and sustainability goals in surgical settings, though they must meet stringent regulatory standards for reprocessing and safety.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- medacta.us.com
- —
- —
- [email protected]
- Phone
- 901-203-3470
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 772462123
Catalogue (438)
Page 9 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ComposiTCP | ComposiTCP 30 flat head | FDA UDI | Class II | Active |
| Ligafix | LIGAFIX 30 round head | FDA UDI | Class II | Unknown |
| Ligafix | LIGAFIX 60 round head | FDA UDI | Class II | Active |
| Ligafix | Super elastic guide pin X5 | FDA UDI | Class I | Active |
| Ligafix | LIGAFIX 60 round head | FDA UDI | Class II | Active |
| Bio1-Kit | BIO1-KIT pre-loaded syringe with Ø3 mm granules | FDA UDI | Class II | Unknown |
| FIXIT / ecoFIX | Punch - 3.5 mm | FDA UDI | Class I | Active |
| ComposiTCP | ComposiTCP 30 round head | FDA UDI | Class II | Active |
| Biosorb | BIO1 Cubes | FDA UDI | Class II | Unknown |
| Ligafix | LIGAFIX 60 round head | FDA UDI | Class II | Active |
| Ligafix | LIGAFIX L 60 mm - diameter 11 mm cannulated drill bit, longflute | FDA UDI | Class I | Active |
| Neotis | NEOTIS | FDA UDI | Class II | Unknown |
| Rigidloop | T Adjustable Cortical System - XL | FDA UDI | Class II | Active |
| Otis | Handle | FDA UDI | Class I | Active |
| Biosorb | OTIS | FDA UDI | Class II | Unknown |
| ecoFIX Needle | ecoFIX® Needle Ø 5.5 mm Threaded Double-Loaded Suture Anchor System | FDA UDI | Class II | Active |
| Menix | MENIX complete instrumentation set | FDA UDI | Class I | Active |
| ComposiTCP™ | Double loaded BroadBand suture anchor | FDA UDI | Class II | Active |
| Ligafix | LIGAFIX 60 round head | FDA UDI | Class II | Active |
| Biosorb | BIO1 Cubes | FDA UDI | Class II | Unknown |
| Ligafix | LIGAFIX 30 round head | FDA UDI | Class II | Active |
| ecoFIX Band | ecoFIX® Band Ø 5.5 mm Threaded Double-Loaded Flat Suture Anchor | FDA UDI | Class II | Active |
| ComposiTCP | ComposiTCP 30 round head | FDA UDI | Class II | Unknown |
| RetroTech | Drill bit | FDA UDI | Class I | Active |
| ComposiTCP | ComposiTCP 30 flat head | FDA UDI | Class II | Active |
| Wizard Tcp | BIO1 Granules | FDA UDI | Class II | Active |
| ComposiTCP™ | Suture Anchor Punch Tap | FDA UDI | Class II | Active |
| Otis-C Plus | NON STERILE OTIS-C PLUS Plate | FDA UDI | Class II | Unknown |
| ecoFIX Knotless | ecoFIX® Knotless Ø 6.5 mm Threaded Anchor | FDA UDI | Class II | Active |
| Biosorb | BIO1 Cylinder | FDA UDI | Class II | Unknown |
| FIXIT & ecoFIX | Punch Tap - 4.5 mm | FDA UDI | Class I | Active |
| ComposiTCP | ComposiTCP 30 round head | FDA UDI | Class II | Unknown |
| SoftLink™ | Titanium Button w/Adjustable UHMWPE Loop - cortical tunnel = Ø 5 to 10 mm | FDA UDI | Class II | Unknown |
| Otis-F | OTIS-F AO Ø 6.5 mm tap | FDA UDI | Class I | Active |
| Bio1-Kit | BIO1-KIT pre-loaded syringe with Ø1.5 mm granules | FDA UDI | Class II | Unknown |
| Otis-C-Plus & Otis-F | Drill guide | FDA UDI | Class I | Active |
| MBlock | Adjustable Loop XL | FDA UDI | Class II | Active |
| Bio1-Kit | BIO1-KIT pre-loaded syringe with Ø1.5 mm granules | FDA UDI | Class II | Unknown |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.