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Endoplus

FDA UDI

Class II (US FDA UDI)

by Endoplus

Identity

Trade Name
Endoplus FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
5mm Tri-Grasper Insert, Bariatric Length FDA UDI
Model / Reference
336VL FDA UDI
Description
5mm Tri-Grasper Insert, Bariatric Length FDA UDI

Identifiers

Primary DI / UDI-DI
00817401021097 FDA UDI
510(k) Number
K151567 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

Endoplus by Endoplus — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Cleared under the same submission

K151567 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endoplus

Sources (1)

  • FDA UDI a17a9aaf-1564-4ee8-a0cc-a266854bb4f8 34 fields · synced Jun 7, 2026