AccessGUDID - DEVICE: Flight Dental Systems (D178CLAVE28)

GUDID

Device Identifier (DI) Information

Brand Name: Flight Dental Systems
Version or Model: Clave28+
Commercial Distribution Status: In Commercial Distribution
Catalog Number: Clave28+
Company Name: Flight Dental Systems USA Inc.

Primary DI Number: D178CLAVE28
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 119439759 *Terms of Use

Device Description: The Clave28+ from Flight Dental Systems is a high-capacity Class S steam sterilizer designed to meet the sterilization needs of busy dental and medical practices. With a spacious 28-liter chamber, the Clave28+ offers efficient and reliable sterilization for solid, unwrapped instruments and other general-use items, making it ideal for clinics that require fast turnaround and dependable performance.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
38671	Steam sterilizer	A mains electricity (AC-powered) device designed for total elimination and/or inactivation of microorganisms from medical devices and related products using pressurized steam (i.e., moist heat) as the sterilizing agent; it is used for products non-sensitive to high temperature, water, or steam. It typically includes a treatment chamber with shelves for device placement, and controls; it may be intended to sterilize wrapped and/or unwrapped devices. The device is available in a variety of shapes and sizes, including stand-alone (bulk) and tabletop units.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FLE	Sterilizer, Steam

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K243994	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 42011795-48cf-443e-9d5b-d4cddde54a48
Public Version Date: July 28, 2025
Public Version Number: 1
DI Record Publish Date: July 18, 2025