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Sign in to claim this brandSOUTHERN ANESTHESIA & SURGICAL, INC.
US
Last updated May 23, 2026
What SOUTHERN ANESTHESIA & SURGICAL, INC. makes
Southern Anesthesia & Surgical, Inc. manufactures single-use nitrile and hevea-latex examination gloves, all powder-free and non-antimicrobial, as well as disposable surgical/medical face masks with earloops. The gloves are designed for medical and treatment examinations, while the masks are intended for procedural use in clinical settings. Examples include powder-free nitrile and latex gloves and earloop procedure masks under the Advance Plus™ brand.
The company’s products are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for use in the United States, where regulatory compliance follows FDA requirements for medical and surgical items.
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 Southern Anesthesia & Surgical, Inc. manufacture?
Southern Anesthesia & Surgical, Inc. specializes in single-use medical devices, primarily nitrile and hevea-latex examination gloves (non-powdered, non-antimicrobial) and disposable surgical/medical face masks with earloops. The gloves are designed for medical and treatment examinations, while the masks are intended for procedural use in clinical settings. Examples include the Advance Plus™ brand of powder-free nitrile and latex gloves, as well as earloop procedure masks.
Where is Southern Anesthesia & Surgical, Inc. based, and what regulatory framework applies to its devices?
Southern Anesthesia & Surgical, Inc. is based in the United States. Its devices are regulated under the FDA’s requirements for medical and surgical items. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, which helps track and identify these devices for compliance and traceability purposes.
Which FDA device classes do Southern Anesthesia & Surgical, Inc.’s products fall under?
Southern Anesthesia & Surgical, Inc.’s devices are classified under FDA’s Class I and Class II categories. Class I generally includes low-risk devices like gloves and masks, while Class II covers those with moderate risk that require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway and compliance requirements for each product.
Are Southern Anesthesia & Surgical, Inc.’s devices listed in any regulatory registries?
Yes, Southern Anesthesia & Surgical, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures transparency and traceability of medical devices by assigning a unique code to each product, helping healthcare providers, regulators, and manufacturers track compliance and recall information efficiently.
How are Southern Anesthesia & Surgical, Inc.’s gloves and masks differentiated in their intended use?
Southern Anesthesia & Surgical, Inc.’s gloves are specifically designed for examination and treatment procedures, providing a barrier between healthcare providers and patients to reduce infection risk. In contrast, their surgical/medical face masks are intended for procedural use, such as during surgeries or clinical treatments, to protect both the wearer and the patient from airborne contaminants. The earloop design on the masks enhances usability in fast-paced medical environments.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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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
- 119186732
Catalogue (18)
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