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Deep2 CALYX - CUPPING HP DEEP2

by Termosalud, S.L.

Deep2 CALYX - CUPPING HP DEEP2 (A488) is a Class I device made by Termosalud, S.L., listed in FDA GUDID since 21 Oct 2024 (UDI-DI 00850060304095), registry data as of 12 Nov 2026.

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

Source GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850060304095 UDI-DI Date21 Oct 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Deep2
Generic name
Multi-modality skin surface treatment system
Model / Ref / Catalog
CALYX - CUPPING HP DEEP2, A488
Primary DI / UDI-DI
00850060304095
FDA product code
GFE
GMDN term
Multi-modality skin surface treatment system
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multi-modality skin surface treatment system

Similar devices in this category

Other devices filed under Multi-modality skin surface treatment system.

Other devices from Termosalud, S.L.

See all devices from Termosalud, S.L. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)