510(k) Report

510(k) · Cleared

Cleared

Dental Air Polishing Handpiece

K221548510(k) TraditionalCleared Sep 28, 2022124-day reviewClass I21 CFR 872.4200

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

Guilin Woodpecker Medical Instrument Co., Ltd. · EFB Handpiece, Air-Powered, Dental

Cleared on Sep 28, 2022 as substantially equivalent to K151912 (E.M.S Electro Medical Systems S.A, 2016) after a 124-day review. Its family tree reaches back 7 generations to 1990.

Decided
Sep 28, 2022
Review
124 days
Class
Class I
Product code
EFB
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K900709 (1990). 18 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 7 generations backK900709 Air Flow SiiElectro Medical Systems (Ems Sa) · 1990
  2. 6 generations backK991857 Airflow HandyElectro Medical Systems, Inc. · 1999
  3. 5 generations backK022119 Ems Air-Flow Handy 2 Dental HandpieceElectro Medical Systems SA · 2002
  4. 4 generations backK092289 Ems Air-Flow Handy PerioE.M.S Electro Medical Systems S.A · 2009
  5. 3 generations backK110173 Ems Air-Flow Master PiezonE.M.S Electro Medical Systems S.A · 2011
  6. 2 generations backK132478 Air-Flow Handy 3.0E.M.S Electro Medical Systems S.A · 2014
  7. 1 generation backK151912 AIR-FLOW handy 3.0 PLUSE.M.S Electro Medical Systems S.A · 2016
  8. This deviceK221548 Dental Air Polishing HandpieceGuilin Woodpecker Medical Instrument Co., Ltd. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K900709Air Flow SiiElectro Medical Systems (Ems Sa)1990—
−6K991857Airflow HandyElectro Medical Systems, Inc.1999—
−5K022119Ems Air-Flow Handy 2 Dental HandpieceElectro Medical Systems SA2002—
−4K092289Ems Air-Flow Handy PerioE.M.S Electro Medical Systems S.A2009—
−3K110173Ems Air-Flow Master PiezonE.M.S Electro Medical Systems S.A2011—
−2K132478Air-Flow Handy 3.0E.M.S Electro Medical Systems S.A2014—
−1K151912AIR-FLOW handy 3.0 PLUSE.M.S Electro Medical Systems S.A2016—
0 (this device)K221548Dental Air Polishing HandpieceGuilin Woodpecker Medical Instrument Co., Ltd.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199310
199510
199710
200010
200510
200710
200910
201020
201410
FIG. 1 — Lineage of K221548, 1990–2022Source: 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 EFB? 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 EFB device

  1. #1 K262144 DIAMED Handpiece;DIAMED Airmotor;DIAMED…score 13.3 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K151912AIR-FLOW handy 3.0 PLUS
Summary page 4
…EFB Device Class: Class II Predicate Device: E.M.S. Electro Medical Systems S.A. K151912 Device Description: The Dental Air Polishing Handpiece, AP-H Plus is an air driven dental handpiece for the use b…
E.M.S Electro Medical Systems S.A2016—

Also cleared against K151912: 1 other device →

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 32 years and passes through 5 companies; a new generation was cleared every 3.0 years on median.
  • None of the 18 ancestors has a recall.
  • 1 other device also cites its predicate K151912.

How does its category compare?

All EFB devices

EFB Handpiece, Air-Powered, Dental: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · EFB

1in 2025

2007: 122008: 72009: 112010: 82011: 42012: 82013: 32014: 72015: 72016: 32017: 72018: 32019: 32020: 52021: 22022: 52023: 42024: 52025: 12026 (partial year): 4
2007high 12 (2007) · low 1 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EFB

209in 2024

2007: 61 days median2008: 97 days median2009: 120 days median2010: 116 days median2011: 168 days median2012: 130 days median2013: 207 days median2014: 200 days median2015: 296 days median2016: 205 days median2017: 246 days median2018: 210 days median2019: 348 days median2020: 259 days median2022: 430 days median2023: 158 days median2024: 209 days median2026 (partial year): 252 days median
2007high 430 (2022) · low 61 (2007)2026

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

Recalls per year · EFB

No recall names EFB since 2007.

Adverse event reports per year · EFB

83in 2025

2007: 132008: 192009: 402010: 782011: 962012: 972013: 612014: 732015: 872016: 1222017: 1532018: 812019: 1172020: 942021: 1232022: 1572023: 1162024: 1042025: 83
2007high 157 (2022) · low 13 (2007)2025

MAUDE reports naming product code EFB, 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
20071261013
2008797019
200911120040
20108116078
20114168096
20128130097
20133207061
20147200073
20157296087
201632050122
201772460153
20183210081
201933480117
20205259094
20212—0123
202254300157
202341580116
202452090104
20251—083
202642520—

What is it indicated for?

The Dental Air Polishing Handpiece, AP-H Plus is a dental handpiece intended for use in the cleaning and polishing of teeth by the projection of a mixture of water, air, and powder onto the tooth surface. The device removes soft deposits and areas of discoloration and can be used to prepare teeth for dental procedures such as the placement of composite fillings, porcelain inlays, and laminate veneers. The device can be used to clean implant abutments and…

Read the full statement (154 words)

The Dental Air Polishing Handpiece, AP-H Plus is a dental handpiece intended for use in the cleaning and polishing of teeth by the projection of a mixture of water, air, and powder onto the tooth surface. The device removes soft deposits and areas of discoloration and can be used to prepare teeth for dental procedures such as the placement of composite fillings, porcelain inlays, and laminate veneers. The device can be used to clean implant abutments and to clean teeth prior to treatments such as shade matching, fluoridation, and bleaching. The device can also be used to degrease crowns and bridges prior to placement and clean fixed bands and brackets on orthodontic appliances.

The Dental Air Polishing Handpiece, AP-H Plus is intended for patients suffering from periodontal disease.

The Dental Air Polishing Handpiece, AP-H Plus is indicated for the non-surgical removal of subgingival plaque in pockets up to 4 mm after initial periodontal treatment.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K221548: Dental Air Polishing Handpiece.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K221548

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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