510(k) Report

510(k) · Cleared

Cleared

Tetrix Cream

K071483510(k) TraditionalCleared Apr 4, 2008310-day reviewClass U

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

Coria Laboratories, Ltd. · FRO Dressing, Wound, Drug

Cleared on Apr 4, 2008 as substantially equivalent to K024367 (Sinclair Pharmaceuticals, Ltd., 2003) and 1 other predicate after a 310-day review. Its family tree reaches back 3 generations to 1996. 2 later devices descend from it.

Decided
Apr 4, 2008
Review
310 days
Class
Class U
Product code
FRO
Recalls
None
Predicates
2

Its longest line of descent runs back 3 generations to K961758 (1996). 4 ancestors in all. 2 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1997: 1 other ancestor2012: 1 descendant cleared2010: 1 descendant clearedK961758 · Carasyn Hydrogel Wound Products · Carrington Laboratories, Inc. · 1996K024367 · Sinclair Wound and Skin Emulsion · Sinclair Pharmaceuticals, Ltd. · 2003K041342 · Impruv a.I. Cream Wound and Skin Emulsion · Stiefel Laboratories, Inc. · 20051995200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 2 descendants K041342 · Impruv a.I. Cream Wound and Skin Emulsion · Stiefel Laboratories, Inc. · 2005K024367 · Sinclair Wound and Skin Emulsion · Sinclair Pharmaceuticals, Ltd. · 2003K961758 · Carasyn Hydrogel Wound Products · Carrington Laboratories, Inc. · 19960
  1. Root · 3 generations backK961758 Carasyn Hydrogel Wound ProductsCarrington Laboratories, Inc. · 1996
  2. 2 generations backK024367 Sinclair Wound and Skin EmulsionSinclair Pharmaceuticals, Ltd. · 2003
  3. 1 generation backK041342 Impruv a.I. Cream Wound and Skin EmulsionStiefel Laboratories, Inc. · 2005
  4. This deviceK071483 Tetrix CreamCoria Laboratories, Ltd. · 2008
  5. Descendant · cites it directly · 0 of its ownK113807 Dexeryl CreamPierre Fabre Medical Devices · 2012
  6. Descendant · cites it directly · 0 of its ownK093159 PR CreamPrugen IP Holdings, Inc. · 2010

Most influential descendants

Showing 2 of 2 · See all
  • K113807Dexeryl CreamPierre Fabre Medical Devices · 2012 · cites it directly0descendants
  • K093159PR CreamPrugen IP Holdings, Inc. · 2010 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K961758Carasyn Hydrogel Wound ProductsCarrington Laboratories, Inc.1996—
−2K024367Sinclair Wound and Skin EmulsionSinclair Pharmaceuticals, Ltd.2003—
−1K041342Impruv a.I. Cream Wound and Skin EmulsionStiefel Laboratories, Inc.2005—
0 (this device)K071483Tetrix CreamCoria Laboratories, Ltd.2008—
+1K113807Dexeryl CreamPierre Fabre Medical Devices2012—
+1K093159PR CreamPrugen IP Holdings, Inc.2010—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201210
FIG. 1 — Lineage of K071483, 1996–2012Source: 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 FRO? 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 FRO device

  1. #1 K261023 Microdacyn Wound Irrigation Solutionscore 15.5 · 14 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? (2)

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
*K024367Sinclair Wound and Skin Emulsion
Summary page 1
…ssing, wound and burn, hydrogen w/drug and/or biologic 2.3 Devices to Which New Device is Substantially Equivalent Sinclair Wound K024367 marketed as AtopiClair TM and Skin Emulsion Nonsteroidal Cream Mimyx T M…
Sinclair Pharmaceuticals, Ltd.2003—
*K041342Impruv a.I. Cream Wound and Skin Emulsion
Summary page 1
…K024367 marketed as AtopiClair TM and Skin Emulsion Nonsteroidal Cream Mimyx T M Cream K041342 2.4 Device Description TetrixTM Cream is a non-sterile cream formulation intended for prescription use only.…
Stiefel Laboratories, Inc.2005—

Also cleared against K024367: 9 other devices →

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K113807Dexeryl CreamPierre Fabre Medical Devices20120
K093159PR CreamPrugen IP Holdings, Inc.20100

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 12 years and passes through 4 companies; a new generation was cleared every 2.7 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K113807 (Pierre Fabre Medical Devices, 2012) has gone furthest, with 0 descendants of its own.
  • 9 other devices also cite its predicate K024367.

How does its category compare?

All FRO devices

FRO Dressing, Wound, Drug: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · FRO

11in 2025

2007: 292008: 262009: 312010: 312011: 272012: 242013: 192014: 222015: 282016: 282017: 232018: 202019: 162020: 122021: 82022: 92023: 182024: 242025: 112026 (partial year): 17
2007high 31 (2009) · low 8 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FRO

176in 2025

2007: 187 days median2008: 130 days median2009: 136 days median2010: 146 days median2011: 177 days median2012: 96 days median2013: 194 days median2014: 214 days median2015: 249 days median2016: 222 days median2017: 147 days median2018: 206 days median2019: 270 days median2020: 226 days median2021: 275 days median2022: 332 days median2023: 283 days median2024: 263 days median2025: 176 days median2026 (partial year): 254 days median
2007high 332 (2022) · low 96 (2012)2026

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

Recalls per year · FRO

2in 2024

2007: 42008: 12009: 12011: 42013: 12014: 12015: 22016: 32017: 12019: 12021: 62022: 22023: 2, 2 Class I2024: 22026 (partial year): 2
2007high 6 (2021) · low 0 (2010)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · FRO

192in 2025

2007: 552008: 302009: 452010: 1222011: 422012: 652013: 1392014: 2692015: 2972016: 1472017: 1492018: 1282019: 1362020: 1392021: 1832022: 1762023: 1982024: 2322025: 192
2007high 297 (2015) · low 30 (2008)2025

MAUDE reports naming product code FRO, 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
200729187455
200826130130
200931136145
2010311460122
201127177442
20122496065
2013191941139
2014222141269
2015282492297
2016282223147
2017231471149
2018202060128
2019162701136
2020122260139
202182756183
202293322176
2023182832 (2)198
2024242632232
2025111760192
2026172542—

What is it indicated for?

TetrixTM Cream is indicated to manage and relieve the burning and itching experienced with various types of dermatoses, including atopic dermatitis, allergic contact dermatitis and irritant contact dermatitis. Tetrix TM Cream helps to relieve dry, waxy skin by maintaining a moist wound and skin environment, which is beneficial to the healing process.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K071483: Tetrix Cream.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K071483

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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