Inman Medical Corp.: FDA filings under this applicant name
FDA lists 14 510(k) clearances under the applicant name “Inman Medical Corp.” (first 1991, latest 1994), across 9 product codes in 4 review panels. Median 510(k) review time under this name: 148 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 |
|---|---|---|---|
| FRO | Dressing, Wound, Drug | 3 | 3 |
| GCY | Apparatus, Suction, Single Patient Use, Portable, Nonpowered | 3 | 3 |
| GCS | Endoscope, Battery-Powered And Accessories | 2 | 2 |
| FER | Anoscope And Accessories | 1 | 1 |
| GCJ | Laparoscope, General & Plastic Surgery | 1 | 1 |
| HIF | Insufflator, Laparoscopic | 1 | 1 |
| KDC | Instrument, Surgical, Disposable | 1 | 1 |
| KKX | Drape, Surgical, Antimicrobial | 1 | 1 |
| KYZ | Syringe, Irrigating (Non Dental) | 1 | 1 |
Review panels
- General and Plastic Surgery (8)
- Gastroenterology and Urology (3)
- General Hospital (2)
- Obstetrics and Gynecology (1)
Most recent Inman Medical Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K933171 | INMAN IRRIGATION TAPERED PROBE | KYZ | 1994-04-29 | 304 |
| K933169 | INMAN ENDOSCOPIC BLUNT DISSECTOR | GCJ | 1994-04-19 | 294 |
| K933094 | INSUFFLATOR TUBING KIT W/FILTER | HIF | 1994-04-18 | 298 |
| K933382 | IMC CABLE/WIRE COVER | KKX | 1994-01-27 | 199 |
| K933774 | IMC SALINE WET DRESSING | FRO | 1993-11-08 | 97 |
| K933306 | IMC 5.0MM IRRIGATION/ASPIRATION PROBE W/HOLES | GCY | 1993-10-05 | 90 |
| K933305 | IMC 5.0MM IRRIGATION/ASPIRATION PROBE | GCY | 1993-10-05 | 90 |
| K933170 | INMAN POOLE TIP SUCTION PROBE W/TUBING KIT | GCY | 1993-09-16 | 79 |
| K932762 | 10.0MM SUCTION/IRRIGATION PROBE & TUBING KIT | GCS | 1993-08-31 | 84 |
| K933371 | IMC ENDOSCOPIC INSTRUMENT HOLDER | GCS | 1993-08-06 | 28 |
4 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Inman Medical 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 Liebelt Corp. (6 510(k)s)
- Inman Orthodontic Laboratories, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Inman Medical Corp.?
FDA lists 14 510(k) clearances under the applicant name “Inman Medical Corp.” (first 1991, latest 1994), across 9 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 Medical Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Inman Medical Corp. is 148 days.
Which FDA product codes appear under Inman Medical Corp.?
The most frequent FDA product codes under this applicant name are FRO (Dressing, Wound, Drug, 3); GCY (Apparatus, Suction, Single Patient Use, Portable, Nonpowered, 3); GCS (Endoscope, Battery-Powered And Accessories, 2).
Next steps
- See all 14 Inman Medical Corp. clearances with predicates and recalls
- Run predicate analysis for product code FRO, Inman Medical 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.