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FlexStone Basket

FDA UDI

Class II (US FDA UDI)

by EndoTheia, Inc.

Identity

Trade Name
FlexStone Basket FDA UDI
Generic Name
Urinary stone retrieval basket, single-use FDA UDI
Device Name
Single-Use Steerable Basket FDA UDI
Model / Reference
FSA-120-21 FDA UDI
Description
Single-Use Steerable Basket FDA UDI

Identifiers

Primary DI / UDI-DI
G380FSA120210 FDA UDI
FDA Product Code
FFL FDA UDI
GMDN Term
Urinary stone retrieval basket, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4680 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Urinary stone retrieval basket, single-use

FlexStone Basket by EndoTheia, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urinary stone retrieval basket, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
EndoTheia, Inc.

Sources (1)

  • FDA UDI c8ae4fef-d7c4-4d69-8e1c-ab17a7ac8846 33 fields · synced May 30, 2026