Yeti Care

FDA Device Registration & Listing · Fairfield, NJ, US · Registration 3030637172

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
3030637172
FEI Number
3030637172
Entity Name
Yeti Care
City/State/Country
Fairfield, NJ, US
Establishment Address
17A Daniel Road East, Fairfield, NJ 07004, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Yeti Care, Inc. (Owner Number: 10090213)
Owner / Operator Contact Address
P.O. Box 702, Holmdel, NJ 07733, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SmartAid Monitoring System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMI Monitor, Bed Patient General Hospital Class 1 880.2400 2024-02-28

Official Correspondent

Binay Sugla

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Yeti Care, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030637172. Last updated year: 2026. Please use registration number 3030637172 when referencing this establishment in official correspondence.
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