510(k) Report

510(k) · Cleared

Cleared

Safe Secure Sterilization Pouches and Rolls

K242839510(k) TraditionalCleared Oct 16, 202427-day reviewClass II21 CFR 880.6850

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Shenzhen Safesecure Medical Infection Control Tech Co., Ltd. · FRG Wrap, Sterilization

Cleared on Oct 16, 2024 as substantially equivalent to K180139 (Safe Secure Packing Co., Ltd., 2019) after a 27-day review. Its family tree reaches back 7 generations to 1999.

Decided
Oct 16, 2024
Review
27 days
Class
Class II
Product code
FRG
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K990567 (1999). No later device cites it as a predicate yet.

  1. Root · 7 generations backK990567 Global Healthcare Self-Sealing Sterilization PouchGlobal Healthcare, Inc. · 1999
  2. 6 generations backK993764 Medipack See-Through Seal Sterilization PouchMedipack Medical Packaging Mfg. Co. · 1999
  3. 5 generations backK051242 Winner Self Seal Sterilization PouchWinner Medical (Usa), Inc. · 2005
  4. 4 generations backK062704 Sterilization Pouch with IndicatorsWinner Industries (Shenzhen) Co., Ltd. · 2007
  5. 3 generations backK112591 Safe Secure Sterilization Pounch with Steam and Ethylene Oxide…Safe Secure Packaging Co., Ltd. · 2012
  6. 2 generations backK153540 Safe Secure Sterilization Pouch with Steam and Ethylene Oxide…Safe Secure Packaging Co., Ltd. · 2016 · Recalled
  7. 1 generation backK180139 Safe Secure Sterilization Pouches and RollsSafe Secure Packing Co., Ltd. · 2019
  8. This deviceK242839 Safe Secure Sterilization Pouches and RollsShenzhen Safesecure Medical Infection Control Tech Co., Ltd. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K990567Global Healthcare Self-Sealing Sterilization PouchGlobal Healthcare, Inc.1999—
−6K993764Medipack See-Through Seal Sterilization PouchMedipack Medical Packaging Mfg. Co.1999—
−5K051242Winner Self Seal Sterilization PouchWinner Medical (Usa), Inc.2005—
−4K062704Sterilization Pouch with IndicatorsWinner Industries (Shenzhen) Co., Ltd.2007—
−3K112591Safe Secure Sterilization Pounch with Steam and Ethylene Oxide Process…Safe Secure Packaging Co., Ltd.2012—
−2K153540Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process IndicatorsSafe Secure Packaging Co., Ltd.201643
−1K180139Safe Secure Sterilization Pouches and RollsSafe Secure Packing Co., Ltd.2019—
0 (this device)K242839Safe Secure Sterilization Pouches and RollsShenzhen Safesecure Medical Infection Control Tech Co., Ltd.2024—
FIG. 1 — Lineage of K242839, 1999–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FRG? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new FRG device

  1. #1 K234050 HALYARD® ONE-STEP® Sterilization Wrap…score 15.8 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K180139Safe Secure Sterilization Pouches and Rolls
Summary page 7
…RG Subsequent Product Code JOJ Device Class: Class II Classification Panel: General Hospital Predicate Device K180139 - Safe Secure Sterilization Pouches and Rolls Device Description The device is made from porous material printed chemical i…
Safe Secure Packing Co., Ltd.2019—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 25 years and passes through 7 companies; a new generation was cleared every 4.5 years on median.
  • 1 of the 7 ancestors has a recall of any class.

How does its category compare?

All FRG devices

FRG Wrap, Sterilization: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · FRG

9in 2025

2007: 32008: 22009: 42010: 42011: 62012: 102013: 62014: 82015: 122016: 92017: 92018: 52019: 92020: 52021: 42022: 92023: 92024: 112025: 92026 (partial year): 4
2007high 12 (2015) · low 2 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FRG

151in 2025

2007: 182 days median2009: 171 days median2010: 213 days median2011: 110 days median2012: 133 days median2013: 146 days median2014: 177 days median2015: 196 days median2016: 131 days median2017: 260 days median2018: 150 days median2019: 258 days median2020: 122 days median2021: 170 days median2022: 217 days median2023: 230 days median2024: 182 days median2025: 151 days median2026 (partial year): 247 days median
2007high 260 (2017) · low 110 (2011)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FRG

2in 2022

2013: 22017: 292020: 142022: 2
2007high 29 (2017) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · FRG

18in 2025

2007: 12008: 22009: 22011: 122012: 42013: 52014: 132015: 92016: 202017: 72018: 222019: 102020: 212021: 92022: 42023: 132024: 212025: 18
2007high 22 (2018) · low 0 (2010)2025

MAUDE reports naming product code FRG, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007318201
20082—02
2009417102
2010421300
20116110012
20121013304
2013614625
20148177013
20151219609
20169131020
20179260297
20185150022
20199258010
202051221421
2021417009
2022921724
20239230013
202411182021
20259151018
202642470—

What is it indicated for?

Safe Secure Sterilization Pouches and Rolls are intended to be used to enclose another medical device, in a single or double pouch configuration, that is to be sterilized by a health care provider using: Gravity steam at 121°C (250°F) for 30 minutes; 25 minutes dry time Pre-vacuum steam at 132°C (270°F) for 4 minutes; 20 minutes dry time Pre-vacuum steam at 134°C (273°F) for 3 minutes; 20 minutes dry time Pre-vacuum steam at 135°C (275°F) for 3 minutes…

Read the full statement (845 words)

Safe Secure Sterilization Pouches and Rolls are intended to be used to enclose another medical device, in a single or double pouch configuration, that is to be sterilized by a health care provider using:

Gravity steam at 121°C (250°F) for 30 minutes; 25 minutes dry time

Pre-vacuum steam at 132°C (270°F) for 4 minutes; 20 minutes dry time

Pre-vacuum steam at 134°C (273°F) for 3 minutes; 20 minutes dry time

Pre-vacuum steam at 135°C (275°F) for 3 minutes; 16 minutes dry time

Ethylene Oxide (EO) with a concentration of 735 mg/L at 55°C (131°F) and 50% to 80% relative humidity for 60 minutes. Aeration time of 8 hours at 60°C (140°F).

The recommended hydrogen peroxide vapor sterilization cycle is :

Standard Cycle of STERRAD® 100S

Standard cycle and Advanced cycle of STERRAD® NX

Standard cycle, Flex cycle and Express cycle of STERRAD® 100NX

Non Lumen Cycle, Lumen Cycle and Flexible Cycle of V-PRO® maX

The steam and EO device are not intended and has not been validated for sterilization of devices that contain lumens. The hydrogen peroxide device has been validated for devices that contain a lumen listed below:

Standard Cycle of STERRAD® 100S

- inside diameter > 1 mm and length < 125 mm

- inside diameter > 2 mm and length <250 mm

Standard cycle of STERRAD® NX

Single channel stainless steel lumens with:

- Inside diameter > 1 mm and length < 150 mm

- Inside diameter > 2 mm and length <400 mm

Single channel PE/PTFE tubing with:

- Inside diameter > 1 mm and length <350 mm

Advanced cycle of STERRAD® NX

Single channel stainless steel lumens with:

- Inside diameter > 1 mm and length < 500 mm

Single PTFE lumen tubing with:

- Inside diameter > 1 mm and length < 1000 mm

Single channel PE/PTFE flexible endoscopes with:

- Inside diameter > 1 mm and length < 850 mm

Standard cycle of STERRAD® 100NX

Single channel stainless steel lumens with:

- Inside diameter > 0.7 mm and length < 500 mm

Single channel PE/PTFE instruments with:

- Inside diameter > I mm and length < 1000 mm

Flex cycle of STERRAD® 100NX

Single channel PE/PTFE flexible endoscope with:

- Inside diameter > 1 mm and length < 850 mm

Lumen Cycle of V-PRO® maX

Lumened and non-lumened instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors.

Medical devices, including single, dual and triple channeled rigid and semi-rigid endoscopes, with the following configurations:

Single channeled devices with a stainless lumen that is > 0.77mm internal diameter (ID) and < 500mm in length

Dual channeled devices with stainless steel lumens that are > 0.77mm ID and < 527mm in length

Triple channeled devices with stainless steel lumens that are

->1.2 mm ID and <275 mm in length

->1.8 mm ID and <310 mm in length

or

->2.8 mm ID and <317 mm in length

Flexible Cycle of V-PRO® maX

Two flexible endoscopes with a light cord (if not integral to the endoscope) and mat with no additional load. The flexible endoscopes may contain either:

A single lumen that is> 1 mm ID and < 1050 mm in length

Or two lumens with:

- One lumen that is> 1 mm ID and < 990 mm in length

- And the other lumen that is > 1 mm ID and < 850 mm in length

One flexible endoscope with a light cord (if not integral to endoscope) and mat and additional non-lumened instruments including instruments with diffusion-restricted areas such as the hinged portion of forceps or scissors. The flexible endoscopes my contain either:

A single lumen that is> 1 mm ID and < 1050 mm in length

Or two lumens with:

- One lumen that is > 1 mm ID and < 990 mm in length

- And the other lumen that is > 1 mm ID and < 850 mm in length

The external chemical indicators on the pouches/rolls are intended to demonstrate that the device has been exposed to the steam, EO, or hydrogen peroxide sterilization process and to distinguish between processed and unprocessed devices. The chemical indicators change from green to purple or from Pink to Cocoa after exposure to steam, from yellow to brown or from Blue to Brown after exposure to ethylene oxide, and from blue to pink for hydrogen peroxide.

The paper version of the pouch is for Steam and EO. The Tyvek version of the pouch is for hydrogen peroxide sterilization only.

If stored according to the recommended conditions, the products before sterilization have a maximum shelf life of 5 years(for paper pouch) and 2 years(for Tyvek pouch) from the date of manufacture. The pouches are intended to allow sterilization of the enclosed medical device(s) and also to maintain sterility (SAL=10-6).

The subject device is intended and has been validated to maintain sterility of the enclosed devices for 12 months after steam sterilization and 24 months after EO sterilization(for paper pouch), and, 2 years after hydrogen peroxide sterilization (for Tyvek Pouch).

The maximum validated pouch load is 2.64 pounds (1.2kg).

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K242839: Safe Secure Sterilization Pouches and Rolls.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K242839

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026