Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003672078

FEI Number

3003672078

Entity Name

210 INNOVATIONS, LLC

City/State/Country

Groton, CT, US

Establishment Address

210 Leonard Drive, Groton, CT 06340, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

210 INNOVATIONS, LLC (Owner Number: 9049843)

Owner / Operator Contact Address

210 Leonard Drive, --, Groton, CT 06340, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Safetmate

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	2002-02-21

Official Correspondent

David Ritchie

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

210 INNOVATIONS, LLC

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 3003672078. Last updated year: 2026. Please use registration number 3003672078 when referencing this establishment in official correspondence.