← Back to catalogue

osseolink Implant

FDA UDI

Class II (US FDA UDI)

by Osseolink Usa Llc

Identity

Trade Name
osseolink Implant FDA UDI
Generic Name
Steel dental bur, reusable FDA UDI
Device Name
Lindemann Surgical Bur FDA UDI
Model / Reference
PD15 FDA UDI
Description
Lindemann Surgical Bur FDA UDI

Identifiers

Primary DI / UDI-DI
00816273020429 FDA UDI
510(k) Number
K091878 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Steel dental bur, 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: Steel dental bur, reusable

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

Similar devices

Also classified as Steel dental bur, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Osseolink Usa Llc

Sources (1)

  • FDA UDI 3c0e2a1b-6d64-4595-9d65-e7fb65d653d8 36 fields · synced Jun 8, 2026