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Tehlin

FDA UDI

Class I (US FDA UDI)

by Teh Lin Prosthetic & Orthopaedic, Inc.

Identity

Trade Name
TEHLIN FDA UDI
Generic Name
External lower-limb prosthesis structural/alignment component FDA UDI
Device Name
BK RIBBED COSMETIC STOCKING 21" FDA UDI
Model / Reference
G-TCS-RB21 FDA UDI
Description
BK RIBBED COSMETIC STOCKING 21" FDA UDI

Identifiers

Primary DI / UDI-DI
04719883464873 FDA UDI
FDA Product Code
IQQ FDA UDI
GMDN Term
External lower-limb prosthesis structural/alignment component FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3420 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: External lower-limb prosthesis structural/alignment component

Tehlin by Teh Lin Prosthetic & Orthopaedic, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External lower-limb prosthesis structural/alignment component.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teh Lin Prosthetic & Orthopaedic, Inc.

Sources (1)

  • FDA UDI 120a5e17-1735-4904-bb0d-8b9d5fe9e34e 33 fields · synced Jun 8, 2026