Steri-Shield

8 Tie Back Toga with Anti-Reflective Face Shield

Registry build 21.09.26
68manufacturers in China registered for this device type
28catalogue numbers in this listing
4510(k) clearances naming this product code
30recalls on this code

Who Else Makes It

Concentrated in Jiangsu (16), Hubei (13), Anhui (10). 28 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FYA
Manufacturer City Province Registered as Device types
GRI Medical & Electronic Technology Co., Ltd. Jiaxing Zhejiang Contract manufacturer 71
Suzhou Meccan Import and Export Corp. Suzhou Jiangsu Contract manufacturer 71
Principle & Will Biotech (Pinghu) Co., Ltd. Pinghu Zhejiang Contract manufacturer 39
Henan Yadu Industrial Co., Ltd. Changyuan Henan Contract manufacturer 35
Jiangsu JianYu Health Medical Co., Ltd. Changzhou Jiangsu Contract manufacturer 35
Sino Protection (Hefei) Medical Products Co., Ltd. Hefei Anhui Contract manufacturer 18
Exact Medical Manufacturing, Inc. Changzhou Jiangsu Contract manufacturer 17
Kingstar Medical (Xianning) Co., Ltd. Xianning Hubei Contract manufacturer 17
Changzhou Holymed Products Co., Ltd. Changzhou Jiangsu Contract manufacturer 16
Weihai Dishang Medical Technology Co., Ltd. Weihai Shandong Contract manufacturer 16
Lianyungang Bronson Non-woven Products Co., Ltd. Lianyungang Jiangsu Contract manufacturer 16
Heyuan Hong DE Medical Products Co., Ltd. Heyuan Guangdong Contract manufacturer 13

Showing 12 of 68. All 68 manufacturers in China registered for Gown, Surgical

Record

Regulatory record for Steri-Shield
Listed by Stryker GmbH, Switzerland
FDA product code FYA
Device type Gown, Surgical
Device class Class 2
Regulation 21 CFR 878.4040
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2025-02-21

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, manufacturing date
Packaging Pack of 9, pack of 8, pack of 11, pack of 10

Catalogue Numbers

Catalogue numbers for Steri-Shield
Catalogue number Size Status
0424851100 In distribution
0424931200 In distribution
0424841100 In distribution
0424941200 In distribution
0424931000 In distribution
0424951000 In distribution
0424821200 In distribution
0424951100 In distribution
0424721100 In distribution
0424731100 In distribution
0424841200 In distribution
0424951200 In distribution
0424821100 In distribution
0424921000 In distribution
0424851200 In distribution
0424751200 In distribution
0424751100 In distribution
0424941100 In distribution
0424831200 In distribution
0424921200 In distribution
0424741200 In distribution
0424931100 In distribution
0424941000 In distribution
0424741100 In distribution
0424721200 In distribution
0424831100 In distribution
0424731200 In distribution
0424921100 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Medline Medline Industries, Inc. 453
Halyard O&M Halyard, Inc. 248
Novo Health Services, LLC Novo Health Services, LLC 222
Alleset GRI Medical & Electronic Technology Co., Ltd. 214
Convertors Cardinal Health 200, LLC 184
Lac-Mac LAC-MAC Limited 157
Invenio GRI Medical & Electronic Technology Co., Ltd. 126
Exact Medical Manufacturing, Inc. Exact Medical Manufacturing, Inc. 107
ComPel Surgical Gown Standard Textile Co., Inc. 67
Halyard GRI Medical & Electronic Technology Co., Ltd. 55
ComPel MLR Surgical Gown Standard Textile Co., Inc. 38
Medline Industries, Inc. Medline Industries, Inc. 35

Showing 12 of 172. All products under Gown, Surgical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K141095 2014-08-26
K121664 2014-03-10
K040764 2004-04-27
K944393 1995-08-28

Recalls

29 of these are Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34,570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2018-02-23 Class II Nonconforming Material/Component Separation of material layers may occur, causing a potential risk of exposure to contaminants. 34570 total products 2019-05-23
2014-12-22 Class III Error in labeling A single lot (11121171) of Flyte Toga Peel-away X-Large (catalog number 0408-830-100) was labeled with an incorrect expiration date of 2412-12-01. The correct expiration date should have read 2014-12-01. 1530 units (170 cases) 2015-05-05
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 21,660 units (2166 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 9,930 units (993 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 2,980 units (298 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 34,640 units (3,464 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 1,980 units (198 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 2,000 units ( 200 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 7960 units (796 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 88,040 units (8,804 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 3000 units (300 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 48,040 units, ( 4804 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 334,520 units (33,452 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 3,000 units (300 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 5,000 units ( 500 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 25,770 units (2,577 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 3,980 units ( 398 boxes) 2014-04-14
2013-05-23 Class II Nonconforming Material/Component Based on an accelerated aging test for this product packaging, there is an indicator of potential for a breach in the sterile barrier in the header bag and potentially the blue sterilization wrap for togas within the second and third year o 6,990 units ( 699 boxes) 2014-04-14
2012-06-01 Class II Process control The clear tape, that is intended to aid in the prevention of patients fluids from contacting the surgeon/surgical staff through the sleeve seam of the toga, was not applied during the manufacturing process. Stryker has received 5 complaint 23,653 ( past 3 years) 47937 all years 2014-04-14
2012-06-01 Class II Process control The clear tape, that is intended to aid in the prevention of patients fluids from contacting the surgeon/surgical staff through the sleeve seam of the toga, was not applied during the manufacturing process. Stryker has received 5 complaint 16, 846 (last 3 years) 35,492 all years 2014-04-14

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