ASCEND EAGLE, INC.

FDA Device Registration & Listing · Pinole, CA, US · Registration 2954902

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
2954902
FEI Number
3003243726
Entity Name
ASCEND EAGLE, INC.
City/State/Country
Pinole, CA, US
Establishment Address
828 San Pablo Avenue, Pinole, CA 94564, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ASCEND EAGLE, INC. (Owner Number: 9044112)
Owner / Operator Contact Address
828 San Pablo Avenue, --, Pinole, CA 94564, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K092472
PMA Number
N/A

All Registered Proprietary Names

MULTIPLE PRIVATE LABELS Cranberry

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LYY Latex Patient Examination Glove General Hospital Class 1 880.6250 2005-11-02
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2010-12-08

Official Correspondent

Yesenia Estrada

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ASCEND EAGLE, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K894452 Kerala Rubber & Reclaims, Ltd. KRR GLOVE, PATIENT EXAMINATION GLOVES 1989-08-09
K891323 Li Wah-Hong Kong, Inc. LI WAH LATEX EXAMINATION GLOVES 1989-08-31
K891418 C & K Mfg. & Sales Co. LATEX EXAMINATION GLOVES, STYLE 510 LX 1989-06-22
K994255 Pt. Maja Agung Latexindo LATEX EXAMINATION GLOVES-PRE-POWDERED-STERILE 2000-02-07
K892946 Yeou-Fwu Rubber Industrial Co., Ltd. STERILE PATIENT EXAMINATION GLOVES 1989-08-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2954902. Last updated year: 2026. Please use registration number 2954902 when referencing this establishment in official correspondence.
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