VIRIDIS BIOPHARMA PVT. LTD

FDA Device Registration & Listing · Mumbai Maharashtra, IN · Registration 3021578480

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
3021578480
FEI Number
3021578480
Entity Name
VIRIDIS BIOPHARMA PVT. LTD
City/State/Country
Mumbai Maharashtra, IN
Establishment Address
Survey No. 65 & 66, H.No. 3 Pt & 1 Pt, Village Gatesh (BK), Taluka-Wada, Dist-Palghar, Mumbai Maharashtra 421303, IN
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
Viridis Biopharma Pvt. Ltd (Owner Number: 10087542)
Owner / Operator Contact Address
Survey No. 65 & 66, H.No. 3 Pt & 1 Pt, Village Gatesh (BK), Taluka-Wada, Dist-Palghar, Mumbai, IN-MH 421303, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Naked Bandage

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2023-03-13

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Viridis Biopharma Pvt. Ltd
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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021578480. Last updated year: 2026. Please use registration number 3021578480 when referencing this establishment in official correspondence.
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