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BioHorizons

FDA UDI

Class II (US FDA UDI)

by Biohorizons Implant Systems Inc.

Identity

Trade Name
BioHorizons FDA UDI
Generic Name
Dental regeneration membrane fixation tack, non-bioabsorbable FDA UDI
Device Name
AutoTac Titanium Tacks, pkg of 21 & Cassette FDA UDI
Model / Reference
400-260 FDA UDI
Description
AutoTac Titanium Tacks, pkg of 21 & Cassette FDA UDI

Identifiers

Primary DI / UDI-DI
00847236010249 FDA UDI
FDA Product Code
DZL FDA UDI
GMDN Term
Dental regeneration membrane fixation tack, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4880 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental regeneration membrane fixation tack, non-bioabsorbable

BioHorizons by Biohorizons Implant Systems Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental regeneration membrane fixation tack, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 25bb7bcc-8a1e-49d3-a949-f086e7227471 33 fields · synced May 30, 2026