ET FIXTURE TRANSFER IMPRESSION COPING

GUDID 00810125995293

HIOSSEN, INC.

Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 00810125995293
• NIH Device Record Key: 7a132b9b-55af-4146-9cfd-5d16d4971ed3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ET FIXTURE TRANSFER IMPRESSION COPING
• Version Model Number: ETTIS7014NC
• Company DUNS: 796083090
• Company Name: HIOSSEN, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810125995293 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222636

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-01
• Device Publish Date: 2024-06-21

On-Brand Devices [ET FIXTURE TRANSFER IMPRESSION COPING]

• 00814913026107: ETFTI5020SN
• 00814913026091: ETFTI5020SH
• 00814913026084: ETFTI5017SN
• 00814913026077: ETFTI5017SH
• 00814913026060: ETFTI4020MN
• 00814913026053: ETFTI4020MH
• 00814913026046: ETFTI4017MN
• 00814913026039: ETFTI4017MH
• 00814913026008: ETFTI7014SN
• 00814913025995: ETFTI6014SN
• 00814913025988: ETFTI5014SN
• 00814913025971: ETFTI4514SN
• 00814913025964: ETFTI4014SN
• 00814913025957: ETFTI4514MN
• 00814913025940: ETFTI4014MN
• 00814913025933: ETFTI7014SH
• 00814913025926: ETFTI6014SH
• 00814913025919: ETFTI5014SH
• 00814913025902: ETFTI4514SH
• 00814913025896: ETFTI4014SH
• 00814913025889: ETFTI4514MH
• 00814913025872: ETFTI4014MH
• 00814913025865: ETFTI7011SN
• 00814913025858: ETFTI6011SN
• 00814913025841: ETFTI5011SN
• 00814913025834: ETFTI4511SN
• 00814913025827: ETFTI4011SN
• 00814913025810: ETFTI4511MN
• 00814913025803: ETFTI4011MN
• 00814913025797: ETFTI7011SH
• 00814913025780: ETFTI6011SH
• 00814913025773: ETFTI5011SH
• 00814913025766: ETFTI4511SH
• 00814913025759: ETFTI4011SH
• 00814913025742: ETFTI4511MH
• 00814913025735: ETFTI4011MH
• 00810125995293: ETTIS7014NC
• 00810125995231: ETTIM4014NC
• 00810125995187: ETTIS4014C
• 00810125995286: ETTIS6014NC
• 00810125995279: ETTIS5014NC
• 00810125995262: ETTIS4514NC
• 00810125995255: ETTIS4014NC
• 00810125995248: ETTIM4514NC
• 00810125995224: ETTIS7014C
• 00810125995217: ETTIS6014C
• 00810125995200: ETTIS5014C
• 00810125995194: ETTIS4514C
• 00810125995170: ETTIM4514C
• 00810125995163: ETTIM4014C