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Hydrofera Blue HBCC4450

by Hydrofera, LLC

Hydrofera Blue HBCC4450 is a device classified as Unclassified made by Hydrofera, LLC, cleared under FDA 510(k) K013462 on 11 Jan 2002 and listed in FDA GUDID since 16 Dec 2019 (UDI-DI 10854827008346), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K013462

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10854827008346 UDI-DI Date16 Dec 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK013462 Date11 Jan 2002DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K013462 decided 11 Jan 2002 Active
  • FDA GUDID UDI-DI 10854827008346 listed 16 Dec 2019 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K013462
  2. Listed FDA GUDID 10854827008346

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Hydrofera Blue
Generic name
Wound-nonadherent dressing, permeable, antimicrobial
Model / reference
HBCC4450
Primary DI / UDI-DI
10854827008346
510(k) Number
FDA product code
FRO
GMDN term
Wound-nonadherent dressing, permeable, antimicrobial
Device class
U
GUDID distribution status
In Commercial Distribution
Size
Length — 4 Inch
Width — 4 Inch

Similar devices

Other devices filed under FDA product code FRO (Dressing, Wound, Drug).

Other devices from Hydrofera, LLC

See all devices from Hydrofera, LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)