# Chlorophyllic Concepts (Opc) Private Limited (contract manufacturer, Thane Maharashtra, IN): 12 new FDA device listings, incl. shoulder prosthesis, reverse configuration

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Chlorophyllic Concepts (Opc) Private Limited |
| Owner / operator | Chlorophyllic Concepts (OPC)Private Limited |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer); Export Device to the United States But Perform No Other Operation on Device |
| Location | Thane Maharashtra, IN |
| New listings | 12 |
| Devices | Shoulder Prosthesis, Reverse Configuration; Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented; Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer; Blade, Saw, General & Plastic Surgery, Surgical; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented; Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate; Ankle Fusion Cage; Rod, Fixation, Intramedullary And Accessories |
| Product codes | PHX, KWS, HSN, GFA, LPH, OQG, LZO, MEH, SAI, HSB, MDM |
| Device classes | Class I, Class II |
| Medical specialties | Orthopedic, General, Plastic Surgery |
| First new listing | 2026-07-29 |
| Latest new listing | 2026-09-01 |
| FDA registration number | 3048515471 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.