DermaSensor 10101

by Dermasensor, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00850017786004 UDI-DI	Date9 Sep 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: DermaSensor
Generic Name: Dermatological elastic scattering spectroscopy probe
Model / Reference: 10101

Primary DI / UDI-DI: 00850017786004
De Novo Number: DEN230008
FDA Product Code: QZS
GMDN Term: Dermatological elastic scattering spectroscopy probe

Device Class: Class II
Regulation Number: 878.1830
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Unsafe

Other devices from Dermasensor, Inc.

DermaSensor

Class II

Properties

Serial Number

Other properties (13)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Lot / Batch Number: No
Expiration Date: No
Manufacturing Date: No