FDA product code · Dental · Class 1

EGS: Handpiece, Contra- And Right-Angle Attachment, Dental

EGS is FDA's product code for "Handpiece, Contra- And Right-Angle Attachment, Dental": a Class 1 device classified under 21 CFR 872.4200, reviewed by the Dental panel.

510(k) review time for EGS

Across 14 510(k) clearances under EGS decided from 2018-01-01 to 2026-10-06, the median was 198 days from FDA receipt to decision. Half took between 100 and 265 days, and 80% were decided within 274 days. These are past clearances, not a forecast for a new submission.

Days from FDA receipt to 510(k) decision, EGS, decisions 2018-01-01 to 2026-10-06 (n = 14)
Fastest27
25th percentile100
Median198
75th percentile265
80th percentile274
90th percentile368
Slowest415

Source: openFDA 510(k) records, snapshot of 2026-10-06 (openFDA data as of 2026-09-28). Compare 510(k) review times across all device types, see every code side by side in the Clearance Timeline Estimator, or browse the clearances themselves in PredicateScope.

EGS in the public FDA record

Records naming EGS, from openFDA (snapshot of 2026-09-15)
510(k) clearances, all years73
Establishment listings165
GUDID device identifiers1,459

Counts of records, not of devices or events. Adverse event reports for EGS are in MAUDEScope, as counts with the query shown: MAUDE has no denominator, so a report count is not a rate and does not show that a device caused an event.

FDA-recognized standards that cite EGS

10 FDA recognized consensus standards cite EGS, 3 of them recognized only in part, among them ISO 9168 Third edition 2009-07-15; ISO 7405 Third edition 2018-10 Corrected version 2018-12; IEC 80601-2-60 Edition 2.0 2019-06. Horizontal standards such as biocompatibility, sterilization and software standards can apply without citing the code.

  • 4-180 ISO 9168 Third edition 2009-07-15 — Dentistry - Hose connectors for air driven dental handpieces
  • 4-261 ISO 7405 Third edition 2018-10 Corrected version 2018-12 — Dentistry - Evaluation of biocompatibility of medical devices used in dentistry
  • 4-262 IEC 80601-2-60 Edition 2.0 2019-06 — Medical electrical equipment - Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment
  • 4-269 ISO 3964 Third edition 11-2016 — Dentistry - Coupling dimensions for handpiece connectors [Including AMENDMENT 1 (2018)]
  • 4-276 ISO 14457 Second edition 2017-10 (partial recognition) — Dentistry - Handpieces and motors
  • 4-281 ISO 1797 Third Edition 2017-05 — Dentistry - Shanks for rotary and oscillating instruments
  • 4-305 ISO 10637 Second edition 2018-05 (partial recognition) — Dentistry - Central suction source equipment
  • 4-306 ISO 22052 First edition 2020-06 (partial recognition) — Dentistry - Compressed air source equipment
  • 4-317 ISO 8325 Third edition 2023-03 — Dentistry - Test methods for rotary instruments
  • 4-395 ISO 21850-1 First edition 2020-04 — Dentistry - Materials for dental instruments - Part 1: Stainless steel

Source: FDA Recognized Consensus Standards, snapshot of 2026-09-01. Search them all in the Consensus Standards Lookup.

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