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BellaTform Applicator NG609899D

by Inbella Medical, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850055552494 UDI-DI Date2 Apr 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
BellaTform Applicator
Generic Name
Multi-modality skin surface treatment system
Model / Reference
NG609899D
Primary DI / UDI-DI
00850055552494
510(k) Number
FDA Product Code
GZJ, IPF, PBX
GMDN Term
Multi-modality skin surface treatment system
Device Class
Class II
Regulation Number
882.5890, 890.5850, 878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K250200)

Other devices from Inbella Medical, Inc.

See all devices from Inbella Medical, Inc. →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

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