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Ligaclip

FDA UDI

Class II (US FDA UDI)

by Ethicon Endo-Surgery, Inc.

Identity

Trade Name
LIGACLIP FDA UDI
Generic Name
Ligation clip, metallic FDA UDI
Device Name
LIGACLIP EXTRA Ligating Clip Cartridges: 20 Titanium Clips/ Cartridge (Small) FDA UDI
Model / Reference
LT102 FDA UDI
Description
LIGACLIP EXTRA Ligating Clip Cartridges: 20 Titanium Clips/ Cartridge (Small) FDA UDI

Identifiers

Catalog Number
LT102 FDA UDI
Primary DI / UDI-DI
10705036012795 FDA UDI
510(k) Number
K830503 FDA UDI
FDA Product Code
FZP FDA UDI
GMDN Term
Ligation clip, metallic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4300 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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Ligation clip, metallic

Ligaclip by Ethicon Endo-Surgery, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ligation clip, metallic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 61ac739d-faf1-4471-87b3-a474826bb6f9 36 fields · synced Jun 1, 2026