Jaykay Enterprises Limited has informed stock exchanges about an investigation notice received by its subsidiary from regulatory authorities. The disclosure was made on May 01, 2026, in compliance with SEBI listing regulations and follows an earlier intimation dated June 19, 2025.

Investigation Notice Details

Neumesh Labs Private Limited, a subsidiary of Jaykay Enterprises, received a notice of investigation from the Office of the Regional Director (Northern Region), Ministry of Corporate Affairs (MCA) on April 30, 2026. The notice seeks information and documents for examination purposes.

Company Response and Compliance

The company stated that Neumesh Labs will extend necessary cooperation to the authorities and is currently in the process of submitting the required information and documents sought by MCA. The disclosure was signed by Company Secretary and Compliance Officer Shikha Rastogi and communicated to both BSE Limited and National Stock Exchange of India Ltd.

Regulatory Filing Requirements

The disclosure was made pursuant to Regulation 30 read with Para A of Part A of Schedule III of the SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015. The company also referenced SEBI Master Circular No. HO/49/14/14(7)2025-CFD-POD2/1/3762/2026 dated January 30, 2026 in its filing.

Impact Assessment

According to the disclosure, no specific violation or contravention has been stated in the communication received from MCA. The company has assessed that no immediate material impact has been identified on its financial, operational, or other activities as of the disclosure date.

JK Digital & Advance Systems Private Limited, a wholly owned subsidiary of jaykay enterprises , has been awarded ISO 13485:2016 and ISO 9001:2015 certifications by BSCIC Certifications Private Limited. The certifications were received under Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015, with the disclosure dated April 26, 2026.

Certification Details

The ISO 13485:2016 certification is specifically for Medical Device - Quality Management System, while ISO 9001:2015 covers Quality Management System. Both certifications apply to the manufacture and sale of additive manufactured sterile revision surgery hip implants, augments, spinal implants, and patient-specific implants. The technical area for ISO 13485:2016 includes Non-Active Implants, Non-Active Orthopaedic Implants, A.1.1.12, and Ethylene Oxide Gas Sterilization (EOG), A.1.5.1.

Certificate Validity and Schedule

Both certifications have been issued with the following timeline:

The certificate numbers are BN25082/23560 for ISO 13485:2016 and BN25082/23561 for ISO 9001:2015. Both certificates are subject to annual surveillance audits, and failure to conduct these audits may result in suspension or withdrawal of the certifications.

Business Impact

The receipt of these ISO certifications marks an important milestone for JK Digital's Medical Implants business. The certifications pave the way for end-to-end manufacturing solutions leveraging JK Digital's Additive Manufacturing capabilities. The subsidiary is located at First and Second Floor, Plot 477B, 4th Phase, Peenya Industrial Area, 12th Cross, Bengaluru, Karnataka.