ZIPTEK LLC

FDA Device Registration & Listing · Sarasota, FL, US · Registration 3013722959

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013722959
FEI Number
3013722959
Entity Name
ZIPTEK LLC
City/State/Country
Sarasota, FL, US
Establishment Address
1250 S TAMIAMI TRL STE 303, Sarasota, FL 34239, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ZIPTEK LLC (Owner Number: 10055345)
Owner / Operator Contact Address
1250 S. Tamiami Trail Suite 303, Sarasota, FL 34239, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

zipe

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MAI Fastener, Fixation, Biodegradable, Soft Tissue Orthopedic Class 2 888.3030 2017-07-10
KGS Retention Device, Suture General, Plastic Surgery Class 1 878.4930 2017-07-10
MBI Fastener, Fixation, Nondegradable, Soft Tissue Orthopedic Class 2 888.3040 2017-07-10

Official Correspondent

William Bennett

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ZIPTEK LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K203334 Acuitive Technologies, Inc. The Citrefix Knotless Suture Anchor 2021-02-05
K243467 Osteonic Co., Ltd. Fix2Lock (Biocomposite medial, Biocomposite lateral, Biocombi Self Punching) 2024-12-03
K213415 OSSIO , Ltd. OSSIOfiber Suture Anchor 2022-03-28
K193295 Parcus Medical, LLC Parcus Knotless PEEK and PEEK CF Push-In Suture Anchor 2020-01-23
K193606 Conmed Corporation Y-Knot OneStep Anchor 2020-01-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013722959. Last updated year: 2026. Please use registration number 3013722959 when referencing this establishment in official correspondence.
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