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Sign in to claim this brandWhat IAA SURGICAL INSTRUMENTS COMPANY makes
The company manufactures reusable bronchoscopic biopsy curettes and a range of flexible bronchoscopic forceps, including fenestrated grasping forceps, hook blade scissors, crocodile forceps, reverse grasping forceps, stent removal forceps, measurement forceps, and placement forceps. These tools are designed for endoscopic procedures, with customizable handle shapes and specific shaft dimensions to accommodate procedural needs. Biopsy forceps are also part of the portfolio, tailored for tissue sampling during bronchoscopy.
All listed devices fall under Class I regulation, with their unique device identifiers (UDIs) recorded in the FDA’s UDI database. The company’s products are intended for use within the United States, adhering to applicable regulatory standards for reusable bronchoscopic instruments.
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 IAA Surgical Instruments Company manufacture?
IAA Surgical Instruments Company specializes in reusable bronchoscopic instruments, primarily focused on flexible bronchoscopic biopsy curettes and a variety of forceps. These include fenestrated grasping forceps, hook blade scissors, crocodile forceps, reverse grasping forceps, stent removal forceps, measurement forceps, placement forceps, and biopsy forceps. The devices are designed for endoscopic procedures, with customizable handle shapes and specific shaft dimensions to meet procedural requirements.
Where is IAA Surgical Instruments Company based?
IAA Surgical Instruments Company is based in the United States. This location aligns with the regulatory environment for the devices they manufacture, which are intended for use within the country.
Which regulatory registries list the devices manufactured by IAA Surgical Instruments Company?
The devices produced by IAA Surgical Instruments Company are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for Class I devices, which include their bronchoscopic biopsy curettes and forceps.
How are the devices manufactured by IAA Surgical Instruments Company classified under regulatory standards?
All devices manufactured by IAA Surgical Instruments Company fall under Class I regulation. This classification applies to low-risk medical devices, such as their reusable bronchoscopic forceps and biopsy curettes, which are designed for specific endoscopic procedures. Class I devices typically require less stringent regulatory oversight but still must meet safety and performance standards.
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
- 645387382
Catalogue (8)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Fenestrated Grasping Forceps Handle Type 2 shape follow master sample and custom | BPS2007 | FDA UDI | Class I | Active |
| Hook Blade Scissor Handle Type 2 shape, Shaft Diameter 1.5mm, follow master samp | BPS2004 | FDA UDI | Class I | Active |
| Crocodile Forceps Handle Type 2 shape follow master sample and customer manual | BPS2002 | FDA UDI | Class I | Active |
| Reverse Grasping Forcep, Handle Type 1 shape, Follow master sample and customer | BPS2008 | FDA UDI | Class I | Active |
| Stents Removal Forceps-Working Length 60cm | BPS2003 | FDA UDI | Class I | Active |
| Measurement Forcep, Handle Type like master sample, Follow master sample and cus | BPS2006 | FDA UDI | Class I | Active |
| Placement Forcep, Handle Type 1 shape, Follow master sample and customer manual | BPS2005 | FDA UDI | Class I | Active |
| Biopsy Forceps Handle Type 2 shape follow master sample and customer manual | BPS2001 | FDA UDI | Class I | Active |
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