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Lap-port closure device Bariatric

FDA UDI

Class II (US FDA UDI)

by Orange Surgical Instruments, Llc

Identity

Trade Name
Lap-port closure device Bariatric FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI
Device Name
Lap-port closure device Bariatric FDA UDI
Model / Reference
OSLPCDB FDA UDI
Description
Lap-port closure device Bariatric FDA UDI

Identifiers

Catalog Number
OSLPCDB FDA UDI
Primary DI / UDI-DI
B354OSLPCDB0 FDA UDI
510(k) Number
K101733 FDA UDI
FDA Product Code
GEI FDA UDI
HIF FDA UDI
GCJ FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
884.1730 FDA UDI
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, reusableEndoscopic electrosurgical electrode, monopolar, single-useInsufflation gas conditioning tubing setLaparoscopic wound closure thread

Lap-port closure device Bariatric by Orange Surgical Instruments, Llc — 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

Sources (1)

  • FDA UDI 10432c35-7ea5-4786-9d3c-1af21606ac01 35 fields · synced May 30, 2026