Micro Motors, Inc.: FDA filings under this applicant name
FDA lists 14 510(k) clearances under the applicant name “Micro Motors, Inc.” (first 1990, latest 2000), across 6 product codes in 1 review panel. Median 510(k) review time under this name: 89 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| EFB | Handpiece, Air-Powered, Dental | 7 | 7 |
| EFS | Unit, Oral Irrigation | 2 | 2 |
| ELC | Scaler, Ultrasonic | 2 | 2 |
| DZE | Implant, Endosseous, Root-Form | 1 | 1 |
| EBW | Controller, Foot, Handpiece And Cord | 1 | 1 |
| EIA | Unit, Operative Dental | 1 | 1 |
Review panels
- Dental (14)
Most recent Micro Motors, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K000120 | PRO-TORQ | EBW | 2000-02-03 | 16 |
| K991283 | DYNA TORQ TORQUE WRENCH, TORQUE WRENCH | DZE | 1999-08-18 | 125 |
| K963843 | ELECTRIC SURGICAL IRRIGATION SYSTEM - DUAL CONTROLLER UNIT | EFB | 1997-03-31 | 187 |
| K970002 | STERILE WATER PUMP | EIA | 1997-03-05 | 62 |
| K942380 | MICRO ICS SONIC SCALER | ELC | 1995-08-07 | 445 |
| K935676 | MICRO RSH HIGH SPEED HANDPIECE | EFB | 1995-03-31 | 490 |
| K911068 | 29540 DYNASURG ELECTRIC HANDPIECE AND IRR. SYSTEM | EFB | 1991-05-15 | 65 |
| K903298 | DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP | ELC | 1991-04-16 | 266 |
| K904850 | DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555 | EFS | 1991-01-25 | 88 |
| K896878 | HANDPIECE SYSTEM WITH MOTOR (SEVERAL MODELS) | EFB | 1990-03-08 | 90 |
4 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Micro Motors, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Micro Media Laboratories (52 510(k)s)
- Micro Therapeutics, Inc. (51 510(k)s)
- Micro Therapeutics, Inc. d/b/a ev3 Neurovascular (32 510(k)s)
- Micro Surgical Instruments Corp. (15 510(k)s)
- Micro Detect, Inc. (11 510(k)s)
- Micro Direct, Inc. (9 510(k)s)
- Micro Current Technology, Inc. (8 510(k)s)
- Micro Audiometrics Corp. (6 510(k)s)
- Micro Tronics Corp. (6 510(k)s)
- Micro Specialties, Inc. (4 510(k)s)
- Micro Dental Laboratories (3 510(k)s)
- Micro Encapsulation Tech. (3 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Micro Motors, Inc.?
FDA lists 14 510(k) clearances under the applicant name “Micro Motors, Inc.” (first 1990, latest 2000), across 6 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Micro Motors, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Micro Motors, Inc. is 89 days.
Which FDA product codes appear under Micro Motors, Inc.?
The most frequent FDA product codes under this applicant name are EFB (Handpiece, Air-Powered, Dental, 7); EFS (Unit, Oral Irrigation, 2); ELC (Scaler, Ultrasonic, 2).
Next steps
- See all 14 Micro Motors, Inc. clearances with predicates and recalls
- Run predicate analysis for product code EFB, Micro Motors, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.