Medical Device Manufacturer · IN , Bengaluru

Turtle Shell Technologies Private Limited - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Turtle Shell Technologies Private Limited has 1 FDA 510(k) cleared medical devices. Based in Bengaluru, IN.

Last cleared in 2022. Active since 2022. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Turtle Shell Technologies Private Limited Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hammond Clinical Trial Consulting, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Turtle Shell Technologies Private Limited

1 devices

1-1 of 1

Cleared CT Dec 15, 2022

Dozee VS

K221555 · BZQ

Anesthesiology · 198d

Regulatory Intelligence

Linked clinical trials FDA-regulated device evidence

Regulatory consultant 510(k) submission support ecosystem

Hammond Clinical Trial Consulting, LLC

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Clinical validation data available

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 20, 2026

Turtle Shell Technologies Private Limited - FDA 510(k) Cleared Devices

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