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Sign in to claim this brandGryphon Brands Inc.
US
Last updated May 23, 2026
What Gryphon Brands Inc. makes
Gryphon Brands Inc. manufactures surgical and examination garment kits designed for use in clinical and procedural settings. These kits include sterile drapes, gowns, and other protective garments intended to maintain aseptic conditions during medical procedures.
The company’s products are classified as Class I devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
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 Gryphon Brands Inc. manufacture?
Gryphon Brands Inc. specializes in surgical and examination garment kits. These kits are designed for clinical and procedural environments, including sterile drapes and gowns, which help maintain aseptic conditions during medical procedures. The focus is on protective garments essential for patient and staff safety in healthcare settings.
Where is Gryphon Brands Inc. based, and how does that affect its devices?
Gryphon Brands Inc. is headquartered in the United States. This location means its devices are subject to U.S. regulatory requirements, including classification under the FDA’s system. The company’s products are designed and manufactured in compliance with these standards, ensuring they meet the necessary safety and performance criteria for use in U.S. healthcare settings.
Which regulatory registries list Gryphon Brands Inc.’s devices?
Gryphon Brands Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices in the U.S., ensuring transparency and traceability for healthcare providers, regulators, and patients. Listing in this database is a requirement for Class I devices under FDA regulations.
How are Gryphon Brands Inc.’s devices classified under U.S. regulations?
Gryphon Brands Inc.’s devices are classified as Class I under FDA regulations. This classification is typically assigned to low-risk devices that pose minimal potential harm to users. The classification is determined based on the device’s intended use and risk profile, and it requires less stringent premarket review compared to higher-risk categories.
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
- 118545648
Catalogue (39)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Gryphon Brands | G-N506-BL-2X | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4202-2X | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4014-XL | FDA UDI | Class I | Active |
| Gryphon Brands | VIN-4108-LG | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4070-LG | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4015-2X | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4011-SM | FDA UDI | Class I | Active |
| Gryphon Brands | G-N503-BL-MD | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4071-XL | FDA UDI | Class I | Active |
| Gryphon Brands | G-N504-BL-LG | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4184-LG | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4009-XL | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4003-LG | FDA UDI | Class I | Active |
| Gryphon Brands | G-N502-BL-SM | FDA UDI | Class I | Active |
| Gryphon Brands | VIN-4109-XL | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4010-2X | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4005-2X | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4182-SM | FDA UDI | Class I | Active |
| Gryphon Brands | G-N501-BL-XS | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4185-XL | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4007-MD | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4006-SM | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4004-XL | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4186-2X | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4200-LG | FDA UDI | Class I | Active |
| Gryphon Brands | G-N505-BL-XL | FDA UDI | Class I | Active |
| Gryphon Brands | VIN-4107-MD | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4198-SM | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4068-SM | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4013-LG | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4201-XL | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4012-MD | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4001-SM | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4199-MD | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4008-LG | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4069-MD | FDA UDI | Class I | Active |
| Gryphon Brands | VIN-4106-SM | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4183-MD | FDA UDI | Class I | Active |
| Gryphon Brands | NIT-4002-MD | FDA UDI | Class I | Active |
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