Litton Dental Products: FDA filings under this applicant name
FDA lists 12 510(k) clearances under the applicant name “Litton Dental Products” (first 1976, latest 1979), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 9 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 |
|---|---|---|---|
| ELC | Scaler, Ultrasonic | 7 | 7 |
| EIA | Unit, Operative Dental | 3 | 3 |
| EFB | Handpiece, Air-Powered, Dental | 2 | 2 |
Review panels
- Dental (12)
Most recent Litton Dental Products 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K791704 | MASTERSCALE II | ELC | 1979-10-26 | 59 |
| K791024 | ULTRASONIC DENTAL PROPHYLAXIS UNIT | ELC | 1979-09-17 | 110 |
| K781114 | ULTRAMATE 990 | EIA | 1978-08-14 | 42 |
| K781044 | ULTRASONIC DENTAL PROPHYLAXIS UNIT,SSM | ELC | 1978-06-30 | 8 |
| K772244 | ILLUMINATED DENTAL HANDPIECE | EFB | 1978-01-20 | 42 |
| K771556 | EXR | ELC | 1977-08-22 | 10 |
| K771557 | ULTRASON 990 | ELC | 1977-08-19 | 7 |
| K771252 | CB600, TURBINE CONTROL BOL | EIA | 1977-07-15 | 4 |
| K771251 | HU:500, HYGIENASSIST | EIA | 1977-07-15 | 4 |
| K761247 | LT:200, LOVING TOUCH | ELC | 1976-12-16 | 3 |
2 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Litton Dental Products.
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.
- Litton Medical Electronics (38 510(k)s)
- Litton Bionetics (15 510(k)s)
- Litton Medical Systems (8 510(k)s)
- Litton Datamedix (5 510(k)s)
- Litton Systems, Inc. (4 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Litton Dental Products?
FDA lists 12 510(k) clearances under the applicant name “Litton Dental Products” (first 1976, latest 1979), across 3 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 Litton Dental Products?
The median time from FDA receipt to decision across 510(k)s cleared under the name Litton Dental Products is 9 days.
Which FDA product codes appear under Litton Dental Products?
The most frequent FDA product codes under this applicant name are ELC (Scaler, Ultrasonic, 7); EIA (Unit, Operative Dental, 3); EFB (Handpiece, Air-Powered, Dental, 2).
Next steps
- See all 12 Litton Dental Products clearances with predicates and recalls
- Run predicate analysis for product code ELC, Litton Dental Products'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.