Sterilucent™ Sterilant Disc

Catalogue number SL001, listed by Sterilucent, Inc., United States, under Sterilizer, Chemical. 2 manufacturers in China are registered for this product code.

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (1), Zhejiang (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MLR
Manufacturer City Province Registered as Device types
Ningbo Incote Precision Machinery Co., Ltd. Ningbo Zhejiang Contract manufacturer 2
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106

Record

Regulatory record for Sterilucent™ Sterilant Disc
Listed by Sterilucent, Inc., United States
FDA product code MLR
Device type Sterilizer, Chemical
Device class Class 2
Regulation 21 CFR 880.6860
Record published 2020-04-29
Record revised 2025-09-12 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment temperature 50 to 86 °F
Packaging 5-pack ref sl001 of 5, case ref sl279 of 5
Distribution end date 2021-12-01

Catalogue Numbers

Catalogue numbers for Sterilucent™ Sterilant Disc
Catalogue number Size Status
SL001 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Trilogy® Zimmer, Inc. 274
Sterrad™ Advanced Sterilization Products Services Inc. 18
NexGen® Zimmer, Inc. 15
Welch Allyn, Inc. Welch Allyn, Inc. 10
V-PRO Steris Mexico, S. de R.L. de C.V. 7
Amsco V-PRO Steris Mexico, S. de R.L. de C.V. 6
SteroScope Insert Connector Large Assembly, Type 3, Qty 1 Ideate Medical 4
Vaprox Steris Corporation 4
Sterilink™ Plasmapp Co., Ltd. 3
SteroScope Insert Connector Extra Small Assembly, Type R2, Qty 1 Ideate Medical 2
Sterlink™ Plasmapp Co., Ltd. 2
SteroScope Biopsy Connector Assembly, Type R1, Qty 1 Ideate Medical 2

Showing 12 of 34. All products under Sterilizer, Chemical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K190005 2019-09-13
K140464 2014-10-31

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