510(k) Report

510(k) · Cleared

Cleared

Enbio S

K213991510(k) SpecialCleared Feb 22, 202263-day reviewClass II21 CFR 880.6880

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

Enbio Group AG · FLE Sterilizer, Steam

Cleared on Feb 22, 2022 as substantially equivalent to K210279 (Enbio Group AG, 2021) after a 63-day review. Its family tree reaches back 2 generations to 2019. 1 later device descends from it.

Decided
Feb 22, 2022
Review
63 days
Class
Class II
Product code
FLE
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K190062 (2019). 1 later device descends from it, 1 citing it directly.

Descendants, by generation 1 generation forward: 1 descendant K210279 · Enbio S · Enbio Group AG · 2021K190062 · STATCLAVE G4 Chamber Autoclave · Scican, Ltd. · 2019 · recalled0
  1. Root · 2 generations backK190062 STATCLAVE G4 Chamber AutoclaveScican, Ltd. · 2019 · Recalled
  2. 1 generation backK210279 Enbio SEnbio Group AG · 2021
  3. This deviceK213991 Enbio SEnbio Group AG · 2022
  4. Descendant · cites it directly · 0 of its ownK260254 Enbio PROEnbio Group AG · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K260254Enbio PROEnbio Group AG · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K190062STATCLAVE G4 Chamber AutoclaveScican, Ltd.20191
−1K210279Enbio SEnbio Group AG2021—
0 (this device)K213991Enbio SEnbio Group AG2022—
+1K260254Enbio PROEnbio Group AG2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K213991, 2019–2026Source: 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 FLE? 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 FLE device

  1. #1 K250168 Life Ultra 25L Tabletop Mono Chamber Steam…score 12.7 · 8 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
*K210279Enbio S
Summary page 4
…uct Code FLE Regulation Number 21 CFR 880.6880 Review Panel General Hospital 3. Predicate Device Enbio S (K210279) 4. Device Description The Enbio S is an air-removal (pre-vacuum) table-top steam sterilizer intended for use by a…
Enbio Group AG2021—
†K190062STATCLAVE G4 Chamber AutoclaveScican, Ltd.20191

Also cleared against K210279: 1 other device →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K260254Enbio PROEnbio Group AG20260

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 3 years and passes through 2 companies; a new generation was cleared every 2.3 years on median.
  • 1 of the 2 ancestors has a recall of any class.
  • Of its descendants, K260254 (Enbio Group AG, 2026) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K210279.

How does its category compare?

All FLE devices

FLE Sterilizer, Steam: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · FLE

4in 2025

2007: 52008: 12009: 82010: 22011: 52012: 52013: 52014: 22015: 32016: 12017: 32018: 82019: 52020: 22021: 52022: 102023: 72024: 22025: 42026 (partial year): 3
2007high 10 (2022) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FLE

184in 2025

2007: 67 days median2009: 109 days median2011: 141 days median2012: 111 days median2013: 241 days median2015: 302 days median2017: 233 days median2018: 146 days median2019: 192 days median2021: 147 days median2022: 133 days median2023: 88 days median2025: 184 days median2026 (partial year): 85 days median
2007high 302 (2015) · low 67 (2007)2026

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

Recalls per year · FLE

1in 2021

2007: 12008: 12011: 12012: 12013: 22015: 12018: 12019: 22021: 12026 (partial year): 1
2007high 2 (2013) · low 0 (2009)2026

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

Adverse event reports per year · FLE

71in 2025

2007: 192008: 212009: 192010: 202011: 632012: 692013: 1122014: 1132015: 682016: 762017: 632018: 902019: 912020: 872021: 812022: 702023: 662024: 642025: 71
2007high 113 (2014) · low 19 (2007)2025

MAUDE reports naming product code FLE, 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
2007567119
20081—121
20098109019
20102—020
20115141163
20125111169
201352412112
20142—0113
20153302168
20161—076
20173233063
20188146190
20195192291
20202—087
20215147181
202210133070
2023788066
20242—064
20254184071
20263851—

What is it indicated for?

The Enbio S is an air-removal (pre-vacuum) table-top steam sterilizer intended for use by a health care provider to sterilize medical products by means of pressurized steam. It is suitable for the sterilization of dental and medical instruments that are validated to be sterilized by steam. The Enbio S has not been designed to sterilize liquid loads, bio-medical waste or materials not compatible with steam sterilization. The processing of such loads may…

Read the full statement (222 words)

The Enbio S is an air-removal (pre-vacuum) table-top steam sterilizer intended for use by a health care provider to sterilize medical products by means of pressurized steam. It is suitable for the sterilization of dental and medical instruments that are validated to be sterilized by steam. The Enbio S has not been designed to sterilize liquid loads, bio-medical waste or materials not compatible with steam sterilization. The processing of such loads may result in incomplete sterilization and/or damage to the autoclave.

Please refer to the table below for program name, load description, sterilization temperature, exposure time, drying time and maximum load.

Program Name: 134°C — solid objects, small porous objects, simple objects recessed, narrow-clearance items, dental handpieces, and textiles; wrapped and unwrapped. Sterilization temperature: 134°C (273°F); sterilization time: 4 minutes; drying time: 3 minutes; maximum load: 0.5 Kg/1.1 lbs.

Program Name: 121°C — solid objects, small porous objects, simple objects recessed, narrow-clearance items, dental handpieces, textiles, and plastics; wrapped and unwrapped. Sterilization temperature: 121°C (250°F); sterilization time: 30 minutes; drying time: 5 minutes; maximum load: 0.5 Kg/1.1 lbs.

Program Name: 134°C FAST* — solid objects, non-porous objects, simple instruments (such as scissors, handles, pliers, chisels, probes, etc.), and dental handpieces; unwrapped. Sterilization temperature: 134°C (273°F); sterilization time: 4 minutes; drying time: N/A; maximum load: 0.5 Kg/1.1 lbs. *Immediate Use Steam Sterilization cycle

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K213991: Enbio S.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K213991

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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