FOOSIN MEDICAL SUPPLIES INC.LTD

FDA Device Registration & Listing · WEIHAI Shandong, CN · Registration 3006562124

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
3006562124
FEI Number
3006562124
Entity Name
FOOSIN MEDICAL SUPPLIES INC.LTD
City/State/Country
WEIHAI Shandong, CN
Establishment Address
No.8-1, Weigao West Road,Chucun Town, Weihai Torch Hi-tech Science Park, WEIHAI Shandong 264200, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Weigao Group Company Limited (Owner Number: 10025293)
Owner / Operator Contact Address
No.1 Weigao Road, Torch Hi-tech Science Park, 264210 Weihai, Shandong Province, PEOPLE'S REPUBLIC OF CHINA, Weihai, CN-SD 264210, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K201139
PMA Number
N/A

All Registered Proprietary Names

Wego PGLA Poly(lactic-co-glycolic Acid) 910 Suture WEGO-PGLA Absorbable Surgical Suture WEGO-PTFE Nonabsorbable Expanded Polytetrafluoroethylene Surgical Suture Wego PGA Polyglycolic Acid Suture Wego PDO (Monofilament Polydioxanone ) Suture Wego Silk Black Braided Suture Wego Nylon Monofilament Suture Wego Prolene Polypropylene Monofilament Suture WEGO-PGCL Absorbable Surgical Monofilament Suture Wego-Stainless Steel PGLA Rapid PGA Rapid WEGO-PDO Barbed Suture

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 2014-11-26
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid General, Plastic Surgery Class 2 878.4493 2014-11-26
NBY Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene General, Plastic Surgery Class 2 878.5035 2017-08-03
NEW Suture, Surgical, Absorbable, Polydioxanone General, Plastic Surgery Class 2 878.4840 2010-06-25
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid General, Plastic Surgery Class 2 878.4493 2010-06-25
GAP Suture, Nonabsorbable, Silk General, Plastic Surgery Class 2 878.5030 2008-06-11
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2008-06-11
GAR Suture, Nonabsorbable, Synthetic, Polyamide General, Plastic Surgery Class 2 878.5020 2008-06-11
GAW Suture, Nonabsorbable, Synthetic, Polypropylene General, Plastic Surgery Class 2 878.5010 2008-06-11
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid General, Plastic Surgery Class 2 878.4493 2014-03-24
GAQ Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile General, Plastic Surgery Class 2 878.4495 2020-05-18
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid General, Plastic Surgery Class 2 878.4493 2019-01-28
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid General, Plastic Surgery Class 2 878.4493 2019-01-28
NEW Suture, Surgical, Absorbable, Polydioxanone General, Plastic Surgery Class 2 878.4840 2020-11-20

Official Correspondent

Lina Liu

US Agent Details

Marco Mu Business: MID-LINK INTERNATIONAL CO., LTD Email: us.agent@mid-link.net Phone: (702) 2095185

Related Public Records

Same Entity

Weigao Group Company Limited
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3007616112 Weihai Jierui Medical Products Co., Ltd. WEIHAI Shandong, CN
3007084575 ShanDong WeiGao Group Medical Polymer Co., Ltd Weihai Shandong, CN

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
K241486 Covidien Sofsilk™ Coated Braided Silk Suture 2024-12-03
K072322 Smith & Nephew, Inc. ULTRA FAST-FIX AND ULTRA FAST-FIX AB MENISCAL REPAIR SYSTEMS 2007-09-18

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 3006562124. Last updated year: 2026. Please use registration number 3006562124 when referencing this establishment in official correspondence.
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