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Ventralight

FDA UDI

Class II (US FDA UDI)

by Davol Inc.

Identity

Trade Name
VENTRALIGHT FDA UDI
Generic Name
Surgical mesh laparoscopic delivery/positioning device FDA UDI
Device Name
Ventralight ST Mesh with Echo 2 Positioning System, 6" (15 cm), Circle FDA UDI
Model / Reference
5990015 FDA UDI
Description
Ventralight ST Mesh with Echo 2 Positioning System, 6" (15 cm), Circle FDA UDI

Identifiers

Catalog Number
5990015 FDA UDI
Primary DI / UDI-DI
00801741130991 FDA UDI
FDA Product Code
FTL FDA UDI
ORQ FDA UDI
GCJ FDA UDI
GMDN Term
Surgical mesh laparoscopic delivery/positioning device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 15 Centimeter FDA UDI

Category: Extra-gynaecological surgical mesh, composite-polymerSurgical mesh laparoscopic delivery/positioning device

Ventralight by Davol Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical mesh laparoscopic delivery/positioning device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Davol Inc.

Sources (1)

  • FDA UDI 1e9075de-95c6-4d35-b1e9-26b1e456bc05 37 fields · synced May 29, 2026