American Medical Disposable, Inc.: FDA filings under this applicant name
FDA lists 33 510(k) clearances under the applicant name “American Medical Disposable, Inc.” (first 1979, latest 1984), across 13 product codes in 3 review panels. Median 510(k) review time under this name: 29 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 |
|---|---|---|---|
| EFQ | Gauze/Sponge, Internal | 13 | 13 |
| FRO | Dressing, Wound, Drug | 4 | 4 |
| KDD | Kit, Surgical Instrument, Disposable | 3 | 3 |
| FPX | Strip, Adhesive, Closure, Skin | 2 | 2 |
| FPY | Sheet, Burn | 2 | 2 |
| GDY | Gauze/Sponge, Internal, X-Ray Detectable | 2 | 2 |
| FMC | Patient Examination Glove | 1 | 1 |
| GEC | Brush, Scrub, Operating-Room | 1 | 1 |
| ITG | Bandage, Cast | 1 | 1 |
| KGX | Tape And Bandage, Adhesive | 1 | 1 |
Plus 3 more product codes.
Review panels
Most recent American Medical Disposable, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K833735 | AN ODOR ABSORBENT BANDAGE | NAB | 1984-04-23 | 181 |
| K833734 | NEUROLOGICAL SPONGE ON PLASTIC STICK | — | 1984-04-23 | 181 |
| K833731 | BREATHABLE OVERWRAY BANDAGE NON-ELAS | KGX | 1984-01-27 | 94 |
| K833730 | NON ADHERENT BANDAGE/SHEET | FRO | 1984-01-27 | 94 |
| K833729 | ELASTIC BREATHABLE OVER-WRAP BANDAGE | NAD | 1983-12-30 | 66 |
| K833733 | NON - ADHERENT BANDAGE | FRO | 1983-12-27 | 63 |
| K833732 | NON WETTING UNDERCAST PADDING | ITG | 1983-12-12 | 48 |
| K830202 | COTTON BALLS, X-RAY OPAQUED STRUNG & NON | GDY | 1983-02-23 | 34 |
| K830201 | POLYESTER X-RAY DETECTABLE STRUNG-SPONGE | GDY | 1983-02-23 | 34 |
| K803116 | HEAVY DRAINAGE PACK | GEC | 1981-01-28 | 49 |
23 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named American Medical Disposable, 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.
- American Dade (149 510(k)s)
- American Edwards Laboratories (89 510(k)s)
- American Medical Systems, Inc. (82 510(k)s)
- American Bioproducts Co. (79 510(k)s)
- American Monitor Corp. (73 510(k)s)
- American Pharmaseal Div. Ahsc (64 510(k)s)
- American Bentley (59 510(k)s)
- American Hospital Supply Corp. (56 510(k)s)
- American Research Products Co. (56 510(k)s)
- American Orthodontics (46 510(k)s)
- American Diagnostic Corp. (39 510(k)s)
- American Laboratory Supply, Inc. (36 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under American Medical Disposable, Inc.?
FDA lists 33 510(k) clearances under the applicant name “American Medical Disposable, Inc.” (first 1979, latest 1984), across 13 product codes in 3 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 American Medical Disposable, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name American Medical Disposable, Inc. is 29 days.
Which FDA product codes appear under American Medical Disposable, Inc.?
The most frequent FDA product codes under this applicant name are EFQ (Gauze/Sponge, Internal, 13); FRO (Dressing, Wound, Drug, 4); KDD (Kit, Surgical Instrument, Disposable, 3).
Next steps
- See all 33 American Medical Disposable, Inc. clearances with predicates and recalls
- Run predicate analysis for product code EFQ, American Medical Disposable, 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.