← Back to catalogue

Cor-Knot Micro

FDA UDI

Class II (US FDA UDI)

by LSI Solutions, Inc.

Identity

Trade Name
COR-KNOT MICRO FDA UDI
Generic Name
Suture clasp, non-bioabsorbable FDA UDI
Device Name
COR-KNOT® MICRO Twin Pack FDA UDI
Model / Reference
032760 FDA UDI
Description
COR-KNOT® MICRO Twin Pack FDA UDI

Identifiers

Catalog Number
032760 FDA UDI
Primary DI / UDI-DI
00850012846420 FDA UDI
510(k) Number
K202551 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Suture clasp, non-bioabsorbable 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

No

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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Suture clasp, non-bioabsorbable

Cor-Knot Micro by LSI Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suture clasp, non-bioabsorbable.

Cleared under the same submission

K202551 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
LSI Solutions, Inc.

Sources (1)

  • FDA UDI aa204502-c857-43ff-bfdb-e6e7907afdec 36 fields · synced May 30, 2026