TURTLE SHELL TECHNOLOGIES PRIVATE LIMITED

FDA Device Registration & Listing · Bengaluru Karnataka, IN · Registration 3030284974

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
3030284974
FEI Number
3030284974
Entity Name
TURTLE SHELL TECHNOLOGIES PRIVATE LIMITED
City/State/Country
Bengaluru Karnataka, IN
Establishment Address
#40,City Center, Ground and Mezzanine Floor, CMH Road, Indiranagar, Bengaluru Karnataka 560038, IN
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Turtle Shell Technologies Private Limited (Owner Number: 10090062)
Owner / Operator Contact Address
#40,City Center, Ground and Mezzanine Floor, CMH Road, Indiranagar, Bengaluru, IN-KA 560038, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Dozee Home Dozee VS Dozee SE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BZQ Monitor, Breathing Frequency Anesthesiology Class 2 868.2375 2024-02-09

Official Correspondent

Gaurav Parchani

US Agent Details

David Hammond Business: Hammond Clinical Trial Consulting, LLC Email: daveh@hammondctc.com Phone: (206) 3833508

Related Public Records

Same Entity

Turtle Shell Technologies Private Limited
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
K913749 Edentec Corp. EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170 1992-07-02
K771407 Research Development Corp. LUNG VOLUME & PRESSURE MONITOR 1977-08-04
K122223 Philips Medizin Systeme Boeblingen GmbH NEW: INTELLIVUE CL RESPIRATION POD NEW: SPECIALIZED ASSESSORY: MOBILE CL RESP ATTACHMENT MODIFIED: INTELLIVUE PATIENT MO 2013-04-12

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030284974. Last updated year: 2026. Please use registration number 3030284974 when referencing this establishment in official correspondence.
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