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IAA SURGICAL INSTRUMENTS COMPANY

US

Last updated May 30, 2026

Part of Iaa Surgical Instruments Co

What 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
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
645387382

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