APOLLO MEDICAL PRODUCTS CORP.

Apollo Medical Products Corp. specializes in single-use medical devices primarily for surgical and procedural applications. Their portfolio includes general surgical procedure kits (both medicated and non-medicated), surgical soft-tissue manipulation forceps, pellet implantation cannulae, soft-tissue biopsy procedure kits, surgical instrument interim-placement holders, isolation gowns, and oral care kits. These devices are designed for one-time use to ensure sterility and reduce infection risks in clinical settings.

Apollo Medical Products Corp. is based in the United States. All of their listed devices are manufactured domestically, adhering to regulatory standards for medical device production in the country.

Apollo Medical Products Corp.’s devices are listed under the FDA’s UDI (Unique Device Identification) system. This system assigns a unique identifier to each medical device to improve tracking, transparency, and regulatory oversight in the healthcare industry.

Apollo Medical Products Corp.’s devices fall under surgical and procedural classifications, as they are designed for use in surgical procedures, tissue manipulation, biopsy, and infection control (e.g., isolation gowns). Classification under regulatory frameworks like the FDA’s UDI system depends on the intended use, risk level, and procedural context of each device type.

Apollo Medical Products Corp.’s general surgical procedure kits are differentiated by their single-use design, which ensures sterility and reduces cross-contamination risks. They are available in both medicated and non-medicated variants, catering to specific procedural needs such as antiseptic treatment or clean-field applications. The kits are part of a broader portfolio tailored for procedural efficiency and safety in clinical environments.