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osseolink Implant

FDA UDI

Class II (US FDA UDI)

by Osseolink Usa Llc

Identity

Trade Name
osseolink Implant FDA UDI
Generic Name
Dental implantation depth/angle gauge, reusable FDA UDI
Device Name
Double Ended Depth Gauge FDA UDI
Model / Reference
DEPG FDA UDI
Description
Double Ended Depth Gauge FDA UDI

Identifiers

Primary DI / UDI-DI
00816273020719 FDA UDI
510(k) Number
K091878 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implantation depth/angle gauge, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Dental implantation depth/angle gauge, reusable

osseolink Implant by Osseolink Usa Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation depth/angle gauge, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Osseolink Usa Llc

Sources (1)

  • FDA UDI fed6d908-3766-45e0-94ab-35e8ec3aa142 36 fields · synced Jun 1, 2026