Inman Liebelt Corp.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Inman Liebelt Corp.” (first 1990, latest 1991), across 6 product codes in 4 review panels. Median 510(k) review time under this name: 80 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 |
|---|---|---|---|
| FAQ | Bag, Urine Collection, Leg, For External Use, Sterile | 1 | 1 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 1 | 1 |
| HDA | Forceps, Obstetrical | 1 | 1 |
| KMK | Device, Intravascular Catheter Securement | 1 | 1 |
| KNY | Accessories, Catheter, G-U | 1 | 1 |
| OCT | Anti Fog Solution And Accessories, Endoscopy | 1 | 1 |
Review panels
- Gastroenterology and Urology (3)
- General Hospital (1)
- Obstetrics and Gynecology (1)
- General and Plastic Surgery (1)
Most recent Inman Liebelt Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K912211 | INTRAVASCULAR CATHETER SECURMENT DEVICE | KMK | 1991-08-09 | 81 |
| K912146 | URETERAL CATHETER HOLDER | KNY | 1991-07-26 | 72 |
| K905590 | UCEZ - STERILE LENS FOG REDUCTION DEVICE | OCT | 1991-05-10 | 148 |
| K905583 | ILC FORCEPS PADS | HDA | 1991-04-12 | 121 |
| K903611 | ILC LEG BAG HOLDER | FAQ | 1990-10-26 | 78 |
| K903610 | O.R. TIP CLEANER | GEI | 1990-10-19 | 71 |
Recalls
openFDA lists no recalls under a recalling firm named Inman Liebelt Corp..
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.
- Inman Medical Corp. (14 510(k)s)
- Inman Orthodontic Laboratories, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Inman Liebelt Corp.?
FDA lists 6 510(k) clearances under the applicant name “Inman Liebelt Corp.” (first 1990, latest 1991), across 6 product codes in 4 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 Inman Liebelt Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Inman Liebelt Corp. is 80 days.
Which FDA product codes appear under Inman Liebelt Corp.?
The most frequent FDA product codes under this applicant name are FAQ (Bag, Urine Collection, Leg, For External Use, Sterile, 1); GEI (Electrosurgical, Cutting & Coagulation & Accessories, 1); HDA (Forceps, Obstetrical, 1).
Next steps
- See all 6 Inman Liebelt Corp. clearances with predicates and recalls
- Run predicate analysis for product code FAQ, Inman Liebelt Corp.'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.