EU MDR • CE • ISO 13485
Surgical Suture Manufacturer Trusted Worldwide
Absorbable and non-absorbable sutures, hernia mesh and haemostats built in our Bengaluru cleanrooms — validated to 1.1× USP strength.
Every suture-needle combination is tested at a minimum of 1.1× USP tensile strength and needle-pull requirements.
Materials, USP sizes, needle geometries and pack formats that let one supplier cover your entire wound-closure catalogue.
ISO 13485 QMS, CE marking and EU MDR certification across 13 product families — audit-ready technical files.
From private-label packs to complete suture plant set-up, our engineers transfer process know-how, not just goods.
Universal Sutures — the flagship brand of Unisur Lifecare Pvt. Ltd. (an LVS Group company) — designs, develops, manufactures and exports surgical sutures, polypropylene hernia mesh, bone wax, oxidized regenerated cellulose, veterinary sutures and laparoscopic devices from Bengaluru, India.
We are proudly the second Indian suture manufacturer to achieve EU MDR (Regulation 2017/745) certification, covering 13 product families in record time. Our purpose is simple and measurable: healing beyond comfort — supported by validated processes, documented batch traceability and a workforce where more than 70% of colleagues are women.
Eight device families covering human and veterinary surgery — available sterile or non-sterile, in branded, generic or OEM configurations.








Universal Sutures is the surgeon’s choice for secure & safe wound closure
Colour-coded by international suture convention — compare material, structure and typical clinical indication before you request technical files.

Plain Catgut — Absorbable

Chromic Catgut — Absorbable

Polyglycolic Acid — Absorbable

Polyglactin 910 — Absorbable

Polydioxanone — Absorbable

Poliglecaprone 25 — Absorbable

Polypropylene — Non-Absorbable

Polyamide (Nylon) — Non-Absorbable

Coated Polyester — Non-Absorbable

UHMWPE Polyethylene — Non-Absorbable

Surgical Bone Wax

Polypropylene Hernia Mesh
A documented quality management system governs raw-material qualification, in-process checks, sterility assurance and batch release — so every shipment arrives with traceable evidence, not assurances.
More than 200 professionals in braiding, needling, packing, QA/QC and regulatory affairs. Complementary skills across the line mean fewer deviations and faster corrective action.
Occupational safety and health practices are aligned with our ISO 13485 framework. We operate a strict no-child-labour policy and prioritise education and skill development for our people.
Country-specific labelling, technical documentation and post-market support help distributors register and defend the product family in their own regulatory jurisdiction.
We design, develop and manufacture virtually any suture, polypropylene mesh or bone wax configuration under your brand — and if you plan to build your own plant, we provide complete turnkey process transfer.
Practical guidance written by our product and regulatory teams for hospital buyers, distributors and OEM brand owners.
Polypropylene, polyester, partially absorbable composites and coated barriers behave very differently in the abdominal wall. A material-by-material comparison.
Read the article →
Fixation method affects positioning, operating time and early repair stability. How to match tacker type to mesh construction and approach.
Read the article →
PLGA tacks secure mesh during healing and then resorb into lactic and glycolic acid — reducing permanent implant burden in minimally invasive repair.
Read the article →Our Bengaluru facility operates under an ISO 13485 quality management system with CE marking and EU MDR (Regulation 2017/745) certification. Universal Sutures is the second Indian suture manufacturer to secure EU MDR certification, covering 13 product families including surgical sutures, bone wax and hernia repair devices. Certificates are published on our certifications page.
Sutures are needled on drilled-end ribbed needles, sealed in aluminium foil primary packs with a validated sterile barrier, then terminally sterilised using validated ethylene oxide cycles. Each batch is released with a certificate of analysis covering tensile strength, needle-attachment pull, sterility and endotoxin limits.
Yes. Our OEM division develops customised suture, mesh and bone wax ranges under your brand — including artwork, multi-language labelling, pack configuration, needle geometry selection and regulatory dossier support. Full details are on the OEM services page.
Every suture and suture-needle combination is manufactured to at least 1.1 times the USP requirement for tensile strength and needle-attachment pull, giving a deliberate safety margin above pharmacopoeial minimums and protecting knot security in demanding closures.
Yes. Beyond standard sheets, we manufacture keyhole, plug and sling configurations, and can supply polypropylene mesh in rolls up to 32 cm width and 25 metres length, sterile or non-sterile, depending on your conversion and registration model.
Our dedicated sutures FAQ library covers absorption profiles, needle codes, USP sizing, storage conditions and shelf life. For product-specific technical files, please reach our team through the contact page.