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Ziptek knotless tissue repair and attachment devices

FDA UDI

Class I (US FDA UDI)

by Ziptek, LLC

Identity

Trade Name
Ziptek knotless tissue repair and attachment devices FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
Ziptek large stainless steel driver/handle assembly reusable medical grade stainless steel ofr use with large 5.0mm screws and biocomposite plugs and as ZipE capture/button pusher FDA UDI
Model / Reference
B56-793-S_D FDA UDI
Description
Ziptek large stainless steel driver/handle assembly reusable medical grade stainless steel ofr use with large 5.0mm screws and biocomposite plugs and as ZipE capture/button pusher FDA UDI

Identifiers

Catalog Number
01 FDA UDI
Primary DI / UDI-DI
00858816006101 FDA UDI
FDA Product Code
LRZ FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

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: Surgical instrument handle, non-torque-limiting

Ziptek knotless tissue repair and attachment devices by Ziptek, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ziptek, LLC

Sources (1)

  • FDA UDI 39019050-a1cf-4b99-acf7-3ea764574120 34 fields · synced May 30, 2026