MERIL ENDO SURGERY PVT. LTD.

FDA Device Registration & Listing · Vapi Gujarat, IN · Registration 3007205024

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
3007205024
FEI Number
3007205024
Entity Name
MERIL ENDO SURGERY PVT. LTD.
City/State/Country
Vapi Gujarat, IN
Establishment Address
Meril Campus, B. No. 8 - F3 and B. No. 6 - F0, F1, F4, Muktanand Marg, Vapi Gujarat 396191, IN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Meril Endo Surgery Pvt. Ltd. (Owner Number: 10051260)
Owner / Operator Contact Address
Meril Campus, B. No. 8 - F3 and B. No. 6 - F0, F1, F4, Muktanand Marg, Vapi, IN-GJ 396191, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PINION™ PDO Knotless Suture - Absorbable Poly (P-Dioxanone) Knotless Suture PINION™ PGA-PCL Knotless Suture - Absorbable Poly (Glycolide-Co-Caprolactone) Knotless Suture MERIGLU™- Topical Skin Adhesive Skinstich Excel Mirus™ Ligating Clip Mirus™ Ligating Clip Applier Mirus™ Hemorrhoidal Circular Stapler Mirus™ Linear Stapler and Reload Mirus™ Circular Stapler Mirus™ Linear Cutter and Reload Pediex Velocril Filapron Filaxyn Mitsu Mitsu FST DECORI ARYA ARYA FA MELODY Megasorb Monofil MERIL-BONE WAX™ Chromic Gut REDIGUT® PLAIN PRO REDILENE® PRO MERISOFT™ PLAIN™ REDISILK® PRO MERISOFT CHROMIC™ REDIBOND® PRO REDISORB® FAST PRO REDISORB® PRO REDIGUT® CHROMIC PRO REDICAPRONE® - 25 PRO REDIDIOX® PRO REDILON® PRO Plain Gut

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid General, Plastic Surgery Class 2 878.4493 2026-03-10
NEW Suture, Surgical, Absorbable, Polydioxanone General, Plastic Surgery Class 2 878.4840 2026-03-10
MPN Tissue Adhesive For The Topical Approximation Of Skin General, Plastic Surgery Class 2 878.4010 2025-01-22
GAG Stapler, Surgical General Hospital Class 2 878.4740 2021-10-28
FZP Clip, Implantable General, Plastic Surgery Class 2 878.4300 2021-10-28
GDW Staple, Implantable General, Plastic Surgery Class 2 878.4750 2021-10-28
NEW Suture, Surgical, Absorbable, Polydioxanone General, Plastic Surgery Class 2 878.4840 2017-11-03
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid General, Plastic Surgery Class 2 878.4493 2017-11-03
MTJ Wax, Bone Unknown Class U N/A 2025-07-10
GAO Suture, Nonabsorbable General, Plastic Surgery Class 2 878.4495 2019-07-25
GAR Suture, Nonabsorbable, Synthetic, Polyamide General, Plastic Surgery Class 2 878.5020 2019-07-25
HMN Suture, Nonabsorable, Ophthalmic Unknown Class 3 N/A 2019-07-25
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid General, Plastic Surgery Class 2 878.4493 2019-07-25
GAN Suture, Absorbable, Synthetic General, Plastic Surgery Class 2 878.4830 2019-07-25
GAP Suture, Nonabsorbable, Silk General, Plastic Surgery Class 2 878.5030 2019-07-25
GAS Suture, Nonabsorbable, Synthetic, Polyester General, Plastic Surgery Class 2 878.5000 2019-07-25
GAL Suture, Absorbable, Natural General, Plastic Surgery Class 2 878.4830 2019-07-25
GAW Suture, Nonabsorbable, Synthetic, Polypropylene General, Plastic Surgery Class 2 878.5010 2019-07-25

Official Correspondent

Umesh Sharma

US Agent Details

Kaiyumkhan Patel Business: Meril Inc. Email: kaiyum.patel@merillife.com Phone: (267) 5158405

Related Public Records

Same Entity

Meril Endo Surgery 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
K123940 Demetech Corp. DEMEQUICKTM (RAPID ABSORBABLE) SYNTHETIC SURGICAL SUTURE 2014-05-30
K050845 ETHICON, Inc. MONOCRYL PLUS ANTIBACTERIAL SUTURE 2005-06-29
K221629 Covidien Tri-Staple™ 2.0 Black Circular Reloads (for use with Signia™ Circular Adapters) 2023-02-22
K231491 Covidien TA™ Stapler and Loading Unit with DST Series™ Technology 2023-08-16
K131563 Opus Ksd, Inc. SUBQ IT! BIOABSORBABLE SKIN CLOSURE SYSTEM 2014-04-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0010-2021 Riverpoint Medical, LLC 2
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 6/0 Undyed 18" P-10 Cutting, Product Number: SV9913, UDI: 20884521153278 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.
Z-0011-2021 Riverpoint Medical, LLC 2
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" P-14 Cutting, Product Number: SV935, UDI: 20884521151755 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.
Z-0012-2021 Riverpoint Medical, LLC 2
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" P-12 Cutting, Product Number: SV426, UDI: 20884521151731 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.
Z-0013-2021 Riverpoint Medical, LLC 2
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36" KV-34 TaperCutting, Product Number: CV919, UDI: 20884521151649 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.
Z-0014-2021 Riverpoint Medical, LLC 2
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" C-12 Cutting, Product Number: SV2294, UDI 20884521151403 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007205024. Last updated year: 2026. Please use registration number 3007205024 when referencing this establishment in official correspondence.
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