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Anchor Pin

FDA UDI

Class II (US FDA UDI)

by Biopro, Inc.

Identity

Trade Name
ANCHOR PIN FDA UDI
Generic Name
Intraoperative bone pin/screw, non-sterile FDA UDI
Model / Reference
17647 FDA UDI

Identifiers

Primary DI / UDI-DI
00810012483766 FDA UDI
510(k) Number
K061798 FDA UDI
FDA Product Code
HTY FDA UDI
GMDN Term
Intraoperative bone pin/screw, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intraoperative bone pin/screw, non-sterile

Anchor Pin by Biopro, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraoperative bone pin/screw, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biopro, Inc.

Sources (1)

  • FDA UDI f5049eee-f112-4de2-b74f-d0ac6a7a8210 33 fields · synced May 30, 2026