Data / Medical devices / India / Chlorophyllic Concepts (opc) Private Limited

Chlorophyllic Concepts (opc) Private Limited: FDA-registered device maker in Thane Maharashtra, India, 4 510(k) clearances

Name: Chlorophyllic Concepts (opc) Private Limited FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Chlorophyllic Concepts (opc) Private Limited is registered with the FDA (registration 3048515471) in Thane Maharashtra, India. It lists 11 device types. The FDA files 4 510(k) clearances under its listings, the newest dated December 5, 2025. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch Chlorophyllic Concepts (opc) Private Limited

FDA registration number: 3048515471
Address: Shop 11, Pujit Plaza, Sector 11 CBD Belapur, Navi Mumbai, Thane Maharashtra, India, 400614
Owner or operator: Chlorophyllic Concepts (OPC)Private Limited (10096222)
Roles: Contract manufacturer, Exporter to the US
First device listed: July 29, 2026
Registered through: 2026

Devices it lists

Device	Product code	Class	Role	Source
Ankle Fusion Cage	SAI	2	Exporter to the US	accessdata.fda.gov
Blade, Saw, General & Plastic Surgery, Surgical	GFA	1	Exporter to the US	accessdata.fda.gov
Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented	OQG	2	Exporter to the US	accessdata.fda.gov
Instrument, Manual, Surgical, General Use	MDM	1	Exporter to the US	accessdata.fda.gov
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer	HSN	2	Exporter to the US	accessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented	LZO	2	Exporter to the US	accessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented	LPH	2	Exporter to the US	accessdata.fda.gov
Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate	MEH	2	Exporter to the US	accessdata.fda.gov
Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented	KWS	2	Contract manufacturer	accessdata.fda.gov
Rod, Fixation, Intramedullary And Accessories	HSB	2	Exporter to the US	accessdata.fda.gov
Shoulder Prosthesis, Reverse Configuration	PHX	2	Contract manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
December 5, 2025	K252067	Velora Acetabular System	LPH	Substantially Equivalent	Restor3D, Inc.	accessdata.fda.gov
March 24, 2025	K242356	TIDAL Fusion Cage System	SAI	Substantially Equivalent	Restor3D, Inc.	accessdata.fda.gov
November 28, 2023	K232595	Kinos Axiom Total Ankle System	HSN	Substantially Equivalent	Restor3D	accessdata.fda.gov
June 30, 2020	K192778	Kinos Axiom Total Ankle System	HSN	Substantially Equivalent	Kinos Medical	accessdata.fda.gov

Compare with other makers

Updated December 5, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.