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neoClose AnchorGuide 5/15 Port Closure Kit US (2 Port)

FDA UDI

Class II (US FDA UDI)

by Neosurgical, Ltd.

Identity

Trade Name
neoClose AnchorGuide 5/15 Port Closure Kit US (2 Port) FDA UDI
Generic Name
Laparoscopic wound closure thread FDA UDI
Device Name
Laparoscopy wound closure system kit consists of: 05391529640002; neoClose AnchorGuide 5/12 & 8/15 US; Model Number NCA515-U; Qty 10 and 05391529640217; neoClose 4 AutoAnchor Pack US; Model Number NCAA4-U; Qty 10 FDA UDI
Model / Reference
NCAG515(2)-U FDA UDI
Description
Laparoscopy wound closure system kit consists of: 05391529640002; neoClose AnchorGuide 5/12 & 8/15 US; Model Number NCA515-U; Qty 10 and 05391529640217; neoClose 4 AutoAnchor Pack US; Model Number NCAA4-U; Qty 10 FDA UDI

Identifiers

Primary DI / UDI-DI
05391529640224 FDA UDI
510(k) Number
K142903 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic wound closure thread FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laparoscopic wound closure thread

neoClose AnchorGuide 5/15 Port Closure Kit US (2 Port) by Neosurgical, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic wound closure thread.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neosurgical, Ltd.

Sources (1)

  • FDA UDI 20fa8941-b0f9-4268-8e2b-2557e2940d52 34 fields · synced May 30, 2026