MD™ Quick Load®

MD™ QUICK LOAD® SUTURE (2-0 Polyester, Green, Non-absorbable, 38") with Needle Cap Unloader

Registry build 21.09.26
1manufacturer
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Registered in Shanghai.

Chinese manufacturers registered for FDA product code GAS
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106

Record

Regulatory record for MD™ Quick Load®
Listed by LSI Solutions Inc., United States
FDA product code GAS
Device type Suture, Nonabsorbable, Synthetic, Polyester
Device class Class 2
Regulation 21 CFR 878.5000
Establishment Manufacturer
510(k) K203081
Record published 2022-12-22
Record revised 2026-04-13 (version 2)

Specifications

Specifications
MRI safety MR Safe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Case of 12
Sizes Length 38 in

Catalogue Numbers

Catalogue numbers for MD™ Quick Load®
Catalogue number Size Status
023160 Length 38 in In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Atramat Internacional Farmacéutica S.A DE C.V 49
TopLock Fusion Orthopedics, LLC 33
RAM® COR-Suture® Quick Load® LSI Solutions Inc. 15
A.C.S® (Alcon Closure System) Alcon Laboratories, Inc. 10
Riverbond Riverpoint Medical LLC 7
Polybond Riverpoint Medical LLC 6
Fast-FIX Smith & Nephew, Inc. 3
COR-Suture® Quick Load® LSI Solutions Inc. 2
RD® Quick Load® LSI Solutions Inc. 2
GII Ethibond DePuy Mitek, Inc. 2
Rapidloc Ethibond DePuy Mitek, Inc. 2
ALLthread Titanium Biomet Orthopedics 2

Showing 12 of 16. All products under Suture, Nonabsorbable, Synthetic, Polyester

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K203081 2020-11-24
K203120 2020-11-24

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P880094 1989-09-22 DACRON SURGICAL SUTURES Alcon Laboratories, Inc.
P840041 1989-08-08 NOVAFIL(TM) Davis & Geck, Inc.
N83509 1987-02-20 NON-ABSORBABLE (POLYESTER FIBER) SUTURES Davis & Geck, Inc.
N17809 1986-12-03 ETHIBOND* Ethicon, Inc.
N80950 1985-03-22 POLYVIOLENE SUTURE Look, Inc.
N17804 1984-03-27 ETHIBOND* Ethicon, Inc.

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