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Tanses T-32 Series

FDA UDIFDA 510(k)

Class II (US FDA UDI)

510(k) K152412

by Tanses Technologies Inc

Identity

Trade Name
Tanses T-32 Series FDA UDI
Generic Name
Ultraviolet tanning device FDA UDI
Device Name
Tanses T-32 Series tanning bed, model T-32-200, 32 suntan lamps total FDA UDI
Model / Reference
T-32-200 FDA UDI
Description
Tanses T-32 Series tanning bed, model T-32-200, 32 suntan lamps total FDA UDI

Identifiers

Primary DI / UDI-DI
00850056256025 FDA UDI
510(k) Number
K152412 FDA UDI
FDA Product Code
LEJ FDA UDI
GMDN Term
Ultraviolet tanning device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4635 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ultraviolet tanning device

Tanses T-32 Series by Tanses Technologies Inc — Class II — FDA_510K — listed in FDA GUDID, FDA 510(k) — regulatory data on deviCERTS

Similar devices

Also classified as Ultraviolet tanning device.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

FDA Applicant
Tanses Technologies, Inc.

Sources (2)

  • FDA UDI b5ae9b59-6693-4163-a2c5-7326303ce081 59 fields · synced Jun 18, 2026
  • FDA 510(k) K152412 1 fields · synced Jun 9, 2026