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Vertessa Lite 10x22cm

FDA UDI

Class II (US FDA UDI)

by Caldera Medical, Inc.

Identity

Trade Name
Vertessa Lite 10x22cm FDA UDI
Generic Name
Pelvic organ prolapse surgical mesh, composite-polymer FDA UDI
Device Name
Vertessa Lite 10x22cm polypropylene mesh for sacrocolpopexy FDA UDI
Model / Reference
CAL-VL1022 FDA UDI
Description
Vertessa Lite 10x22cm polypropylene mesh for sacrocolpopexy FDA UDI

Identifiers

Primary DI / UDI-DI
00890594000339 FDA UDI
510(k) Number
K150016 FDA UDI
FDA Product Code
OTO FDA UDI
GMDN Term
Pelvic organ prolapse surgical mesh, composite-polymer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 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

Category: Pelvic organ prolapse surgical mesh, composite-polymer

Vertessa Lite 10x22cm by Caldera Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pelvic organ prolapse surgical mesh, composite-polymer.

Cleared under the same submission

K150016 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caldera Medical, Inc.

Sources (1)

  • FDA UDI 84671aa5-c159-49d5-99b4-19e8c8d43493 37 fields · synced May 30, 2026