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Sign in to claim this brandASCEND EAGLE INCORPORATED
US
Last updated May 24, 2026
What ASCEND EAGLE INCORPORATED makes
Ascend Eagle Incorporated manufactures examination and treatment gloves made from nitrile, hevea-latex, polychloroprene, and vinyl materials, all non-powdered and non-antimicrobial. They also produce surgical/medical respirators that are single-use and non-antimicrobial, rubber dams made from hevea-latex, and professional denture repair kits. Additionally, they manufacture an in vitro diagnostic (IVD) control for neurofibromatosis type 1.
The company's devices are classified as Class I and Class II under FDA regulations and are listed in the FDA's Unique Device Identification (FDA UDI) system. Ascend Eagle Incorporated 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 devices does Ascend Eagle Incorporated manufacture?
Ascend Eagle Incorporated manufactures examination and treatment gloves made from nitrile, hevea-latex, polychloroprene, and vinyl materials, all non-powdered and non-antimicrobial. They also produce surgical/medical respirators that are single-use and non-antimicrobial, rubber dams made from hevea-latex, professional denture repair kits, and an in vitro diagnostic (IVD) control for neurofibromatosis type 1.
Where is Ascend Eagle Incorporated based?
Ascend Eagle Incorporated is based in the United States, as stated in the summary section of the device data, which confirms the company's country of origin as US.
Which regulatory registry lists the devices made by Ascend Eagle Incorporated?
The devices manufactured by Ascend Eagle Incorporated are listed in the FDA's Unique Device Identification (FDA UDI) system, as indicated in the LISTED IN field of the device data.
How are the devices made by Ascend Eagle Incorporated classified under FDA regulations?
The devices made by Ascend Eagle Incorporated are classified as Class I and Class II under FDA regulations, as explicitly stated in the DEVICE CLASSES field and reiterated in the summary section of the provided data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- pro2s.com
- —
- —
- [email protected]
- Phone
- 7075536190
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 167102750
Catalogue (324)
Page 7 of 7| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Beesure | BE2815 | FDA UDI | Class I | Active |
| Beesure | BE1158 | FDA UDI | Class I | Active |
| Cranberry | CR3447 | FDA UDI | Class I | Active |
| Cranberry | CR3110_SP | FDA UDI | Class I | Active |
| Beesure | BE601RA | FDA UDI | Class I | Active |
| Beesure | BE2500_SP | FDA UDI | Class I | Active |
| Cranberry | S3090Y | FDA UDI | Class I | Active |
| Cranberry | CR3424 | FDA UDI | Class I | Active |
| Asap | 20301 | FDA UDI | Class I | Active |
| Cranberry | CR3389 | FDA UDI | Class I | Active |
| Cranberry | C2700SP | FDA UDI | Class I | Active |
| Cranberry | CR3117 | FDA UDI | Class I | Active |
| Cranberry | S3160B | FDA UDI | Class I | Active |
| Asap | 20715 | FDA UDI | Class I | Active |
| Cranberry | CR3338 | FDA UDI | Class I | Active |
| Cranberry | CR3206 | FDA UDI | Class I | Active |
| Cranberry | S3090G | FDA UDI | Class I | Active |
| Cranberry | CR3235 | FDA UDI | Class I | Active |
| Beesure | BE1522 | FDA UDI | Class I | Active |
| Cranberry | CR3026 | FDA UDI | Class I | Active |
| Cranberry | CR3579 | FDA UDI | Class I | Active |
| Asap | 20304 | FDA UDI | Class I | Active |
| Asap | 20573 | FDA UDI | Class I | Active |
| Beesure | BE504D | FDA UDI | Class I | Active |
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