FDA product code · Dental · Class 2

EMA: Cement, Dental

EMA is FDA's product code for "Cement, Dental": a Class 2 device classified under 21 CFR 872.3275, reviewed by the Dental panel.

510(k) review time for EMA

Across 51 510(k) clearances under EMA decided from 2018-01-01 to 2026-10-06, the median was 129 days from FDA receipt to decision. Half took between 81 and 235 days, and 80% were decided within 243 days. These are past clearances, not a forecast for a new submission.

Days from FDA receipt to 510(k) decision, EMA, decisions 2018-01-01 to 2026-10-06 (n = 51)
Fastest1
25th percentile81
Median129
75th percentile235
80th percentile243
90th percentile274
Slowest436
Median days by decision year, EMA (years with enough clearances to compute). The partial final year counts only submissions already decided, so its median runs low.
YearMedian daysn
20191277
20201648
20222457
202510610
2026 (to 10-06, partial)1507

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.

EMA in the public FDA record

Records naming EMA, from openFDA (snapshot of 2026-09-15)
510(k) clearances, all years508
Device recalls16
Establishment listings827
GUDID device identifiers3,218

Counts of records, not of devices or events. Adverse event reports for EMA 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 EMA

9 FDA recognized consensus standards cite EMA, among them ISO 9917-1 Second edition 2007-10-01; ISO 29022 First edition 2013-06-01; ISO 7405 Third edition 2018-10 Corrected version 2018-12. Horizontal standards such as biocompatibility, sterilization and software standards can apply without citing the code.

  • 4-153 ISO 9917-1 Second edition 2007-10-01 — Dentistry - Water-based cements - Part 1: Powder/liquid acid-base cements
  • 4-219 ISO 29022 First edition 2013-06-01 — Dentistry - Adhesive - Notched-edge sheer bond strength test
  • 4-261 ISO 7405 Third edition 2018-10 Corrected version 2018-12 — Dentistry - Evaluation of biocompatibility of medical devices used in dentistry
  • 4-295 ANSI ADA Standard No. 41-2020 — Evaluation of Biocompatibility of Medical Devices Used in Dentistry
  • 4-311 ISO 9917-2 Third edition 2017-09 — Dentistry - Water-based cements - Part 2: Resin-modified cements
  • 4-324 ISO TS 16506 First edition 2017-07 Corrected version 2018-03 — Dentistry - Polymer-based luting materials containing adhesive components
  • 4-325 ANSI ADA Standard No. 96-2020 — Dental Water-based Cements
  • 4-348 ISO 9917-1 Third Edition 2025-05 — Dentistry - Water-based cements - Part 1: Acid-base cements
  • 4-364 ISO 3990 First edition 2023-07 — Dentistry - Evaluation of antibacterial activity of dental restorative materials luting materials fissure sealants and orthodontic bonding or luting materials

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

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