Anastoclip Universal Clip Remover

Anastoclip Universal Clip Remover, 6 pack

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code
7recalls on this code

Who Else Makes It

Concentrated in Shanghai (1), Beijing (1), Zhejiang (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FZP
Manufacturer City Province Registered as Device types
Hangzhou Kangji Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Jiangsu Bana Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Beijing Zksk Technology Co., Ltd. Beijing Beijing Contract manufacturer 38

Record

Regulatory record for Anastoclip Universal Clip Remover
Listed by Lemaitre Vascular, Inc., United States
FDA product code FZP
Device type Clip, Implantable
Device class Class 2
Regulation 21 CFR 878.4300
Establishment Manufacturer
510(k) K962043
Record published 2015-06-30
Record revised 2021-04-21 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Anastoclip Universal Clip Remover
Catalogue number Size Status
4001-00 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Weck Teleflex Medical LLC 321
Teleflex Teleflex Medical LLC 57
AtriClip™ LAA Exclusion System Atricure, Inc. 40
Aesculap Aesculap AG 19
Medline Medline Industries, Inc. 15
AtriClip Flex•v Atricure, Inc. 12
E-Pack Ethicon, Inc. 12
AtriClip® Pro•v™ LAA Exclusion System Atricure, Inc. 12
Titanium Ligation Clip Vesocclude Medical, LLC 11
SLS-Clip Vitalitec Surgical 10
SLS-Clip Vitalitec Peters Surgical 10
MirusTM Ligating Clip Meril Endo Surgery PVT. Ltd. 10

Showing 12 of 70. All products under Clip, Implantable

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K173323 2018-03-08
K091987 2010-04-23

Recalls Naming This Product

7 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Anastoclip Universal Clip Remover
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Lemaitre Vascular, Inc. 510(k) number 2016-06-22 Class II Unknown/Undetermined by firm US marketing brochure for the AnastoClip AC Closure
System states that the Anastoclip catalog numbers
can be used for dura closure, but the catalog numbers are only
intended for cardiovascular use
256 units 2021-04-08
Lemaitre Vascular, Inc. 510(k) number 2016-06-22 Class II Unknown/Undetermined by firm US marketing brochure for the AnastoClip AC Closure
System states that the Anastoclip catalog numbers
can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
471 units 2021-04-08
Lemaitre Vascular, Inc. 510(k) number 2016-06-22 Class II Unknown/Undetermined by firm US marketing brochure for the AnastoClip AC Closure
System states that the Anastoclip catalog numbers
can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
170 units 2021-04-08
Lemaitre Vascular, Inc. 510(k) number 2016-06-22 Class II Unknown/Undetermined by firm US marketing brochure for the AnastoClip AC Closure
System states that the Anastoclip catalog numbers
can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
40 units (6-Pack) 2021-04-08
Lemaitre Vascular, Inc. 510(k) number 2016-06-22 Class II Unknown/Undetermined by firm US marketing brochure for the AnastoClip AC Closure
System states that the Anastoclip catalog numbers
can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
39 units 2021-04-08
Lemaitre Vascular, Inc. 510(k) number 2016-06-22 Class II Unknown/Undetermined by firm US marketing brochure for the AnastoClip AC Closure
System states that the Anastoclip catalog numbers
can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
55 units (6 pack) 2021-04-08
Lemaitre Vascular, Inc. 510(k) number 2016-06-22 Class II Unknown/Undetermined by firm US marketing brochure for the AnastoClip AC Closure
System states that the Anastoclip catalog numbers
can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
20 units 2021-04-08

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer