Britt Corp., Inc.: FDA filings under this applicant name
FDA lists 17 510(k) clearances under the applicant name “Britt Corp., Inc.” (first 1979, latest 2001), across 9 product codes in 7 review panels. Median 510(k) review time under this name: 122 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 |
|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | 3 | 3 |
| JOW | Sleeve, Limb, Compressible | 3 | 3 |
| EWG | Laser, Ent Microsurgical Carbon-Dioxide | 2 | 2 |
| HQF | Laser, Ophthalmic | 2 | 2 |
| DPS | Electrocardiograph | 1 | 1 |
| HHR | Laser, Surgical, Gynecologic | 1 | 1 |
| IYO | System, Imaging, Pulsed Echo, Ultrasonic | 1 | 1 |
| LLF | Laser, Neurosurgical, Argon | 1 | 1 |
Plus 1 more product codes.
Review panels
- Cardiovascular (4)
- General and Plastic Surgery (3)
- Ear, Nose and Throat (2)
- Ophthalmic (2)
- Neurology (1)
- Obstetrics and Gynecology (1)
- Radiology (1)
Most recent Britt Corp., Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K003828 | VASO PRESS DVT FOOT GARMENT #VP 520 | JOW | 2001-05-18 | 158 |
| K991038 | VASO PRESS DVT SYSTEM, MODELS VP500, VP501 | JOW | 2000-06-22 | 451 |
| K974393 | VASO PRESS SYSTEM | JOW | 1999-03-19 | 483 |
| K860977 | MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION | LLF | 1986-10-16 | 216 |
| K860975 | MODEL 545-45 LASER FOR EAR, NOSE & THROAT | EWG | 1986-07-18 | 126 |
| K860974 | MODEL 545-45 LASER FOR DERMA., POD., SURGICAL | GEX | 1986-07-07 | 115 |
| K860277 | MODEL 525-25 WATT C02 LASER FOR EAR, NOSE & THROAT | EWG | 1986-05-06 | 99 |
| K860273 | MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY | GEX | 1986-04-23 | 86 |
| K860278 | MODEL 525-25 WATT CO2 LASER FOR DERMA/PLASTIC | GEX | 1986-04-15 | 78 |
| K851425 | MODEL J25-25 WATT CO2 LASER | HHR | 1985-11-12 | 216 |
7 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Britt Corp., 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Britt Corp., Inc.?
FDA lists 17 510(k) clearances under the applicant name “Britt Corp., Inc.” (first 1979, latest 2001), across 9 product codes in 7 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Britt Corp., Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Britt Corp., Inc. is 122 days.
Which FDA product codes appear under Britt Corp., Inc.?
The most frequent FDA product codes under this applicant name are GEX (Powered Laser Surgical Instrument, 3); JOW (Sleeve, Limb, Compressible, 3); EWG (Laser, Ent Microsurgical Carbon-Dioxide, 2).
Next steps
- See all 17 Britt Corp., Inc. clearances with predicates and recalls
- Run predicate analysis for product code GEX, Britt Corp., 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 (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.