Hemorrhage Occluder Pin

FDA UDI

Class II (US FDA UDI)

by Tools For Surgery, Llc

Identity

Trade Name: Hemorrhage Occluder Pin FDA UDI
Generic Name: Skin stapler/staple, non-bioabsorbable FDA UDI
Device Name: Sterile titanium thumbtack designed to control severe sacral bleeding during pelvic surgery. FDA UDI
Model / Reference: HOP-03 FDA UDI
Description: Sterile titanium thumbtack designed to control severe sacral bleeding during pelvic surgery. FDA UDI

Identifiers

Catalog Number: HOP-03 FDA UDI
Primary DI / UDI-DI: 00861838000309 FDA UDI
510(k) Number: K040109 FDA UDI
FDA Product Code: GDW FDA UDI
GMDN Term: Skin stapler/staple, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4750 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 7 Millimeter FDA UDI
Outer Diameter — 10 Millimeter FDA UDI

Category: Skin stapler/staple, non-bioabsorbable

Hemorrhage Occluder Pin by Tools For Surgery, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Skin stapler/staple, non-bioabsorbable.

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Cleared under the same submission

K040109 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Tools For Surgery, Llc

Sources (1)

FDA UDI 65a15e6f-e3d8-4745-97dc-e7b730c9af40 37 fields · synced May 30, 2026