Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013595329

FEI Number

3013595329

Entity Name

Tekna Manufacturing Pvt. Ltd.

City/State/Country

Chennai Tamil Nadu, IN

Establishment Address

C19, Industrial Estate, Guindy, Chennai Tamil Nadu 600032, IN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Tekna Manufacturing Pvt. Ltd (Owner Number: 10045541)

Owner / Operator Contact Address

C19, Industrial Estate, Guindy, Chennai, IN-TN 600032, IN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K002794

PMA Number

N/A

All Registered Proprietary Names

Hybrid 3200 Series Monoplace Hyperbaric Chamber Ultrabaric oxygen treatment hood Modular Multiplace Hyperbaric Chamber Model 5000/XX Series Multiplace Hyperbaric Chamber;

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CBF	Chamber, Hyperbaric	Anesthesiology	Class 2	868.5470	2013-11-27
FOG	Hood, Oxygen, Infant	Anesthesiology	Class 1	868.5700	2020-06-13
CBF	Chamber, Hyperbaric	Anesthesiology	Class 2	868.5470	2013-11-27

Official Correspondent

Sriram Narasimhan

US Agent Details

Wen Wang Business: Willow glen Consultancy llc Email: Wen.Wang@WillowGlenFDA.com Phone: (619) 8690249

Related Public Records

Same Entity

Tekna Manufacturing Pvt. Ltd

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 3013595329. Last updated year: 2026. Please use registration number 3013595329 when referencing this establishment in official correspondence.