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Sign in to claim this brandWhat Bien-Air Surgery SA makes
Bien-Air Surgery SA manufactures single-use and reusable dental and otolaryngology (ENT) burs, including diamond-coated and metal/carbide variants for precision drilling in nasal, sinus, and ear procedures. Their portfolio also includes reusable middle ear drill bits, reciprocating surgical saw blades for cranial applications, and ENT suction dissectors for surgical assistance. Specific products range from micro-burrs for delicate ear work to larger cranial burs and saw blades designed for bone removal or shaping.
The company’s devices are classified under FDA regulations as Class I and Class II, with most products listed in the FDA’s Unique Device Identifier (UDI) database. These instruments are intended for use in surgical and procedural settings within the United States, adhering to applicable medical device standards and manufacturing controls.
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 Bien-Air Surgery SA manufacture?
Bien-Air Surgery SA specializes in surgical instruments primarily used in otolaryngology (ENT) and dental procedures. Their product line includes single-use and reusable diamond-coated and metal/carbide burs for precision drilling in nasal, sinus, and ear surgeries. They also produce reusable middle ear drill bits, reciprocating surgical saw blades for cranial applications, and ENT suction dissectors. These tools are designed for tasks like bone removal, shaping, or delicate dissection in surgical settings.
Where is Bien-Air Surgery SA based, and what does that mean for their regulatory compliance?
Bien-Air Surgery SA is based in the United States. Since their devices are manufactured and marketed here, they must comply with U.S. regulatory requirements, such as FDA registration and classification. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, which helps ensure traceability and adherence to U.S. medical device regulations.
Which regulatory registries list Bien-Air Surgery SA’s devices?
Bien-Air Surgery SA’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a unique product code to each device, enabling better tracking, transparency, and compliance with U.S. regulatory standards. This listing helps healthcare providers and regulators identify and verify the devices in clinical settings.
How are Bien-Air Surgery SA’s devices classified under FDA regulations?
Bien-Air Surgery SA’s devices are classified under two categories by the FDA: Class I and Class II. Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body area it interacts with, such as ENT or cranial procedures.
What kinds of surgical applications are Bien-Air Surgery SA’s burs and drill bits designed for?
Bien-Air Surgery SA’s burs and drill bits are engineered for precision surgical applications in otolaryngology and cranial procedures. Diamond-coated and metal/carbide burs are used for delicate drilling in nasal, sinus, and ear surgeries, while reusable middle ear drill bits and cranial burs are designed for controlled bone removal or shaping. Reciprocating surgical saw blades cater to cranial applications, and ENT suction dissectors assist in surgical navigation and tissue manipulation, ensuring precision in complex procedures.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 481597719
Catalogue (772)
Page 11 of 16| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bur PM2-70 50K Diam C Ø5.0 | 1100435 | FDA UDI | Class I | Active |
| Bur PM2-125 80K matchstick Ø3.0mm sterile | 1100341 | FDA UDI | Class II | Unknown |
| Bur PM2-95 80K steel Ø2.3mm sterile | 1100448 | FDA UDI | Class I | Unknown |
| Bur PM2-70 50K Steel Ø1.4 St | 1100419 | FDA UDI | Class I | Active |
| Bur PM2-70 80K Diam EC Ø6.0 St | 1100382 | FDA UDI | Class II | Active |
| Bur PM2-70 80K diam Ø1.0 St | 1101218 | FDA UDI | Class I | Active |
| 0.7mm S2 Mini Diamond Round Bur | 1502176 | FDA UDI | Class I | Active |
| Bur PM2-70 80K diamond Ø3.1mm sterile | 1100372 | FDA UDI | Class I | Unknown |
| OSSEODOC Control Unit + Pump | 1600331 | FDA UDI | Class II | Active |
| Short Bullnose Blade 22x0.4mm | 1502731-003 | FDA UDI | Class I | Active |
| Tungst.Carb.Burr, Ø2.7x70mm, 50k | 340827 | FDA UDI | Class I | Active |
| Bur PM2-70 50K Steel Ø0.6 St | 1100416 | FDA UDI | Class I | Active |
| ShBlade Straight Ø3.5mm SS St | 1600542 | FDA UDI | Class I | Active |
| Bur PM2-125 80K Steel Ø6.0 St | 1100458 | FDA UDI | Class II | Active |
| Long Microsaw Blade 27x0.6mm | 1502681 | FDA UDI | Class I | Active |
| T.Carb.Micro-Ear-Burr, Ø1.8, 12k | 460818 | FDA UDI | Class I | Active |
| HS Stand. Burr, Ø5.0x125, 80k | 360150 M | FDA UDI | Class II | Active |
| Short Bullnose Blade 27x0.4mm | 1502732-003 | FDA UDI | Class I | Active |
| Set OSSEODUO + S120 | 1700250 | FDA UDI | Class II | Active |
| Bur PM2-70 80K diam Ø0.6 St | 1101216 | FDA UDI | Class I | Active |
| Bur PM2 80K Steel TD Ø1.1x4 St | 1100472 | FDA UDI | Class I | Active |
| Bur PM2-70 80K Carb Ø1.8 St | 1100396 | FDA UDI | Class I | Active |
| Pm Perfo | 1600832 | FDA UDI | Class II | Active |
| Bur PM2-70 80K Carb Ø3.1 St | 1100399 | FDA UDI | Class I | Active |
| Bur Cranial Spiral 25mm St | 1100413 | FDA UDI | Class II | Active |
| OSSEOSTAP Sterilization Tray | 1600669 | FDA UDI | Class I | Active |
| Cranio Guard 15mm rotating | 1600879 | FDA UDI | Class II | Unknown |
| BASCH-1 Micromotor | 1600884 | FDA UDI | Class II | Unknown |
| Bur PM2-70 80K steel twist drill Ø1.1x4mm sterile | 1100472 | FDA UDI | Class II | Unknown |
| Short Microsaw Blade 22x0.4mm | 1502671 | FDA UDI | Class I | Active |
| 80K / RAPIDO / PM PERFO Cable | 1600519 | FDA UDI | Class II | Active |
| HS Stand. Burr, Ø3.1x70, 50k | 340131 | FDA UDI | Class I | Active |
| Bur PM2-95 80K Diam Ø1.0 St | 1100320 | FDA UDI | Class I | Active |
| Bur PM2-70 80K diam Ø3.5 St | 1101224 | FDA UDI | Class I | Active |
| Bur PM2-125 80K steel Ø2.3mm sterile | 1100454 | FDA UDI | Class I | Unknown |
| Bur PM2-125 80K Diam Ø1.8 St | 1100309 | FDA UDI | Class I | Active |
| Bur PM2-95 80K Diam Ø2.3 St | 1100322 | FDA UDI | Class I | Active |
| Short Bullnose Blade 32x0.4mm | 1502733-010 | FDA UDI | Class I | Active |
| Diam. Micro-Ear-Burr, Ø1.2, 12k | 460212 | FDA UDI | Class I | Active |
| Bur PM2-70 50K Carb Xcut Ø2.3 | 1100439 | FDA UDI | Class I | Active |
| HS Diam. Burr, Ø3.1x150, 80k | 360231 L | FDA UDI | Class II | Active |
| Bur PM2-70 80K Carb Ø7.0 St | 1100405 | FDA UDI | Class I | Active |
| OSSEOSTAP Control Unit | 1600686 | FDA UDI | Class II | Active |
| HS-Handpiece, angled, 150mm, 80k | 362684 | FDA UDI | Class II | Active |
| Bur PM2-70 80K steel Ø0.6mm sterile | 1100351 | FDA UDI | Class I | Unknown |
| Bur PM2-150 80K Diam C Ø5.0 St | 1100335 | FDA UDI | Class I | Active |
| Bur PM2-70 80K Carb Ø4.0 St | 1100401 | FDA UDI | Class I | Active |
| Bur PM2-125 80K Drum Ø5x10 St | 1100343 | FDA UDI | Class II | Active |
| Bur PM2-125 80K Diam Ø4.0 St | 1101192 | FDA UDI | Class II | Active |
| Bur OSSEOSTAP Carb Ø0.6 mm St | 1501223 | FDA UDI | Class I | Active |
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